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Reactions (166)
Substances (173)
Targets (168)
Citations (200)
Conditions
References
100
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Rx-ID: 26101945 Find similar reactions
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in further solvent(s) solvent: C6Cl6 or fluorinated hydrocarbons, molar ratio NaH:BPO4=3:1, N2-atmosphere, 280-300°C;;
Thiokol Chemical Corp.
Patent: US2849276 , 1958 ; C. A., 1959 , p. 4670 Full Text Show Details
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
in mineral oil
molar ratio NaH:BPO4=3:1, N2-atmosphere, 280-300°C;;
Thiokol Chemical Corp.
Patent: US2849276 , 1958 ; C. A., 1959 , p. 4670 Full Text Show Details Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
in mineral oil
heating BPO4 with NaH in mineral oil;; cooling, extraction with liquid NH3;;
Thiokol Chemical Corp.
Patent: US2849276 , 1958 ; C., 1963 , p. 14823 Full Text Show Details
Hide Details Gmelin Handbook: P: MVol.C, 266, page 611 - 613 Full Text Show Details
in mineral oil heating BPO4 with NaH in mineral oil;; cooling, extraction with liquid NH3;;
A
B
C
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101
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Rx-ID: 26121819 Find similar reactions
in ammonia
byproducts: NH3; B2H6 reacts as amine;
Parry, R. W.; Shore, S. G.
Journal of the American Chemical Society, 1958 , vol. 80, p. 15 - 20 Full Text View citing articles Show Details
in ammonia
byproducts: NH3; NH3 (liquid); B2H6 reacts as amine;
Gmelin Handbook: Na: SVol.3, 1.5.5, page 947 - 953 Full Text Show Details
A
B
C
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102
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Rx-ID: 26121821 Find similar reactions
in ammonia
byproducts: NH3; B2H6 reacts in liquid NH3 as amine;
Parry, R. W.; Shore, S. G.
Journal of the American Chemical Society, 1958 , vol. 80, p. 15 - 20 Full Text View citing articles Show Details
in ammonia
byproducts: NH3; NH3 (liquid); B2H6 reacts in liquid NH3 as amine;
Gmelin Handbook: Na: SVol.3, 1.5.5, page 947 - 953 Full Text Show Details
103
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Rx-ID: 26149304 Find similar reactions
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in neat (no solvent) byproducts: CaO; react. in an autoclave under H2-pressure, 300-600°C, exothermic react. (formation of CaH2 from CaCl2 and H2 during the react. possible); addn. of SiO2 for absorption of CaO;;
Gmelin Handbook: Na: SVol.1, 61, page 259 - 261 Full Text Show Details
Farbenfabriken Bayer A.-G.
Patent: DE1036222 , 1958 ; C., 1960 , p. 5610 Full Text Show Details
A
B
C
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104
Synthesize Find similar Rx-ID: 26379023 Find similar reactions
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A: >99
140-160°C;
Studiengesellschaft Kohle m.b.H.
Patent: DE1018397 , 1957 ; C., 1960 , p. 5610 Full Text Show Details
Studiengesellschaft Kohle m.b.H.
Patent: DE1035109 , 1958 ; C., 1960 , p. 5610 Full Text Show Details
A: >99
140-160°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A
105
B
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Rx-ID: 26452335 Find similar reactions
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With hydrogen
heating in autoclave under H2 pressure at 300 - 600°C, exotherm react.;
Farbenfabriken Bayer A.-G.
Patent: DE1036222 , 1958 ; C, 1960 , p. 5610 Full Text Show Details
With H2
heating in autoclave under H2 pressure at 300 - 600°C, exotherm react.;
Gmelin Handbook: Na: SVol.3, 3.9.1, page 1262 - 1270 Full Text Show Details
A
B
C
D
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106
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Rx-ID: 26572936 Find similar reactions
Parry, R. W.; Shore, S. G.
Journal of the American Chemical Society, 1958 , vol. 80, p. 15 - 20 Full Text View citing articles Show Details
Shore, S. G.; Parry, R. W.
Journal of the American Chemical Society, 1958 , vol. 80, p. 12 - 15 Full Text View citing articles Show Details
Gmelin Handbook: B: B-Verb.10, 3.2.4, page 42 - 43 Full Text Show Details
in ammonia
107
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Rx-ID: 26101857 Find similar reactions
90%
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With catalyst: Na-alcoholate in neat (no solvent) passing BF3 over NaH in presence of a Na-alcoholate, 250-300°C;;
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Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
E. I. du Pont de Nemours & Co.
Patent: US2684888 , 1954 ; C. A., 1954 , p. 13181 Full Text Show Details
in neat (no solvent) byproducts: B2H6; on passing a mixture of BF3 and H2 (ratio=1:2) over powdered NaH at about 180°C;;
Hurd, D. T.
Journal of the American Chemical Society, 1949 , vol. 71, p. 20 - 22 Full Text View citing articles Show Details
in diethyl ether
react. of NaH with a soln. of BF3 in ether in an autoclave (about 10 at), 24h, about 120°C;;
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Heyl & Co., Chemisch-Pharmazeutische Fabrik
Patent: DE944546 , 1956 ; C. A., 1958 , p. 12341 Full Text Show Details
Heyl & Co., Chemisch-Pharmazeutische Fabrik
Patent: GB711174 , 1954 ; C. A., 1954 , p. 14140 Full Text Show Details
Hide Details
in mineral oil
at 250-265°C;; washing with petroleum ether, extractn. of NaBH4 from the residue with liquid NH3 at -33°C;;
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Callery Chemical Co.
Patent: DE958646 , 1957 ; C., 1957 , p. 10305 Full Text Show Details
Callery Chemical Co.
Patent: GB774728 , 1957 ; C. A., 1957 , p. 14217 Full Text Show Details
in neat (no solvent) byproducts: B2H6; on passing a mixture of BF3 and H2 (ratio=1:2) over powdered NaH at about 180°C;;
Gmelin Handbook: Na: SVol.2, 90, page 801 - 803 Full Text Show Details
108
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Rx-ID: 26101911 Find similar reactions
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Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Callery Chemical Co.
Patent: DE958646 , 1957 ; C., 1957 , p. 10305 Full Text Show Details
Callery Chemical Co.
Patent: GB774728 , 1957 ; C. A., 1957 , p. 14217 Full Text Show Details
in mineral oil
at 250-265°C;; washing with petroleum ether, extractn. of NaBH4 from the residue with liquid NH3 at -33°C;;
A
109
B
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Rx-ID: 26101917 Find similar reactions
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A: 83%
in tetrahydrofuran
with excess NaH; at 65°C;
Gmelin Handbook: B: B-Verb.8, 8.2, page 109 - 115 Full Text Show Details
Petterson, L. L.; Steinberg, H.
in: H. Steinberg, Organoboron Chemistry, Vol. I, Interscience Publishers, John Wiley and Sons Inc., New York London - Sydney 1964, p. 610/24 Full Text Show Details
in tetrahydrofuran
on boiling in THF, pptn. of NaBH4;;
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
Brown, H. C.; Mead, E. J.; Shoaf, C. J.
Journal of the American Chemical Society, 1956 , vol. 78, p. 3616 - 3620 Full Text View citing articles Show Details
in tetrahydrofuran
on boiling in THF, pptn. of NaBH4;;
Brown, H. C.; Mead, E. J.
Journal of the American Chemical Society, 1953 , vol. 75, p. 6263 - 6265 Full Text View citing articles Show Details
Gmelin Handbook: Na: SVol.2, 92, page 805 - 807 Full Text Show Details
110
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Rx-ID: 26101937 Find similar reactions
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in mineral oil
at 250-265°C;; washing with petroleum ether, extractn. of NaBH4 from the residue with liquid NH3 at -33°C;;
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Callery Chemical Co.
Patent: DE958646 , 1957 ; C., 1957 , p. 10305 Full Text Show Details
Callery Chemical Co.
Patent: GB774728 , 1957 ; C. A., 1957 , p. 14217 Full Text Show Details
in neat (no solvent) byproducts: NaOC2H5; molar ratio NaH: B(OC2H5)3=4:1, at 225-275°C in an autoclave, extractn. with liquid NH3 or isopropylamine;; high purity;;
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; C. A., 1951 , p. 4007 Full Text Show Details
A
B
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111
Synthesize Find similar Rx-ID: 26154034 Find similar reactions
with removing of Na<B(OCH3)4>;
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
Gmelin Handbook: B: B-Verb.8, 8.2, page 109 - 115 Full Text Show Details
in tetrahydrofuran
65°C, disproportionation, Na(BH4) insol. precipitation;
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
in diethylene glycol
disproportionation, Na(B(OCH3)4) precipitation;
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
Hide Details
in tetrahydrofuran
disproportion;
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
Brown, H. C.; Mead, E. J.; Shoaf, C. J.
Journal of the American Chemical Society, 1956 , vol. 78, p. 3616 - 3620 Full Text View citing articles Show Details
210-240°C; in vac.;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Gmelin Handbook: B: B-Verb.8, 8.2, page 109 - 115 Full Text Show Details
230°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
in tetrahydrofuran
230°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Gmelin Handbook: B: B-Verb.8, 8.2, page 109 - 115 Full Text Show Details
in tetrahydrofuran
precipitation of Na(BH4);
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
in tetrahydrofuran
in diethylene glycol
230°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Gmelin Handbook: B: B-Verb.8, 8.2, page 109 - 115 Full Text Show Details
in diethylene glycol
precipitation of Na(BH4);
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
in diethylene glycol
Brown, H. C.; Mead, E. J.; Tierney, P. A.
Journal of the American Chemical Society, 1957 , vol. 79, p. 5400 - 5404 Full Text View citing articles Show Details
230°C;
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
in tetrahydrofuran
precipitation of Na(BH4);
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
230°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
in tetrahydrofuran
disproportion;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
in diethylene glycol dimethyl ether
precipitation of Na(BH4);
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
in diethylene glycol dimethyl ether
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
in tetrahydrofuran
65°C, disproportionation, Na(BH4) insol. precipitation;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
in diethylene glycol dimethyl ether
disproportionation, Na(B(OCH3)4) precipitation;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
112
B
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Rx-ID: 26379022 Find similar reactions
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Pearson, R. K.; Edwards, L. J.
N.S.A., CCC-1024-TR-213 (1956) 1/10 1957 , vol. 11, p. 3327 Full Text Show Details
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A
B
C
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113
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Rx-ID: 26461277 Find similar reactions
A: >99
in further solvent(s) in boiling perhydrocumole;
Studiengesellschaft Kohle m.b.H.
Patent: DE1018397 , 1957 ; C., 1959 , p. 11376 Full Text Show Details
A: >99
in further solvent(s) in boiling perhydrocumole;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A
B
C
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114
Synthesize Find similar Rx-ID: 26081972 Find similar reactions
in ammonia
-78°C;
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Koenig, F. J.
N.S.A., MCC-1023-TR-137 (1955) 17 1955 , vol. 9, p. 7262 Full Text Show Details
Koenig, F. J.
N.S.A., MCC-1023-TR-137 (1955) 57 1955 , vol. 9, p. 7262 Full Text Show Details
in ammonia
NH3 (liquid); Na(BH4) separated from NH2BH2 by evaporation and extraction with diethylene glycol dimethyl ether;
Schaeffer, G. W.; Adams, M. D.; Koenig, F. J.
Journal of the American Chemical Society, 1956 , vol. 78, p. 725 - 728 Full Text View citing articles Show Details
in ammonia
NH3 (liquid); -78°C;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Hide Details
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
in ammonia
NH3 (liquid); Na(BH4) separated from NH2BH2 by evaporation and extraction with diethylene glycol dimethyl ether;
115
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Rx-ID: 26091409 Find similar reactions
>99
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Gmelin Handbook: Na: SVol.1, 61, page 259 - 261 Full Text Show Details
Schlesinger, H. I.; Brown, H. c.
Patent: US2461661 , 1949 ; C. A., 1949 , p. 4684 Full Text Show Details
Schlesinger,H. I.
N. S. A., A-796 (1943) 6 1956 , vol. 10, p. 3498 Full Text Show Details
in neat (no solvent) byproducts: B(OCH3)3; begin of react. at -80°C, fast react. at ambient temp., exclusion of air;;
A
B
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116
Synthesize Find similar Rx-ID: 26091410 Find similar reactions
A: >99
exclusion of air, from -80°C to room temp.;
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Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Hoekstra, H. R.
N.S.A., The Preparation and Properties of Alkali Metal Borohydrides, AECD-2144 (1947) 14 1948 , vol. 1, p. 756 Full Text Show Details
Schlesinger, H. I.; Hoekstra, H. R.; Brown, H. C.
115th Meeting Am. Chem. Soc., 1949, Abstr. of Papers, S. 9-1O Full Text Show Details
A: >99
usual temp.; quick reactn.;
A: >99 B: >99
Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2461661 , 1949 ; C.A., 1949 , p. 4684 Full Text Show Details
Hoekstra, H. R.
N.S.A., AECD-2144 (1947) 1/45 1948 , vol. 1, p. 756 Full Text Show Details
Schlesinger, H. I.
N.S.A., A-796 (1943) 5 1956 , vol. 10, p. 3498 Full Text Show Details Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2461661 , 1949 ; C.A., 1949 , p. 4684 Full Text Show Details
Hide Details
A: >99
exclusion of air, from -80°C to room temp.;
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
A: >99
usual temp.; quick reactn.;
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
A: >99
usual temp.; quick reactn.;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A: >99
exclusion of air, from -80°C to room temp.;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A: >99 B: >99
Gmelin Handbook: B: B-Verb.8, 3.2.1, page 53 - 65 Full Text Show Details
A
B
C
D
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117
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Rx-ID: 26101914 Find similar reactions
With hydrogen in cyclohexane
3.49parts NaH, 14 parts B(C2H5)3, 50 parts cyclohexane, 240°C, 210 atm. H2-pressure, 3.5h;;
E. I. du Pont de Nemours
Patent: US2729540 , 1956 ; Full Text Show Details
With H2 in cyclohexane
3.49parts NaH, 14 parts B(C2H5)3, 50 parts cyclohexane, 240°C, 210 atm. H2-pressure, 3.5h;;
Gmelin Handbook: Na: SVol.2, 92, page 805 - 807 Full Text Show Details
118
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Rx-ID: 26101916 Find similar reactions
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Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
E. I. du Pont de Nemours & Co.
Patent: US2729540 , 1956 ; C. A., 1956 , p. 6758 Full Text Show Details
in cyclohexane
heating to about 240°C under H2-pressure, pptn. of NaBH4, filtration;; pure product after extractn. with isopropyl amine;;
A
B
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119
Synthesize Find similar Rx-ID: 26101936 Find similar reactions
120
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in tetrahydrofuran
on boiling;;
Brown, H. C.; Mead, E. J.; Shoaf, C. J.
Journal of the American Chemical Society, 1956 , vol. 78, p. 3616 - 3620 Full Text View citing articles Show Details
in tetrahydrofuran
on boiling;;
Gmelin Handbook: Na: SVol.2, 92, page 805 - 807 Full Text Show Details
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Rx-ID: 26106498 Find similar reactions
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Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2461661 , 1949 ; C.A., 1949 , p. 4684 Full Text Show Details
Hoekstra, H. R.
N.S.A., AECD-2144 (1947) 1/45 1948 , vol. 1, p. 756 Full Text Show Details
Schlesinger, H. I.
N.S.A., A-796 (1943) 5 1956 , vol. 10, p. 3498 Full Text Show Details
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
Gmelin Handbook: B: B-Verb.8, 3.2.1, page 53 - 65 Full Text Show Details
121
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Rx-ID: 26110978 Find similar reactions
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Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Callery Chemical Co.
Patent: US2744810 , 1956 ; C. A., 1956 , p. 13386 Full Text Show Details
in neat (no solvent) spraying molten Na with H2 of 150-300°C in a room with BF3;;
A
122
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B
Synthesize Find similar Rx-ID: 26121497 Find similar reactions
B: >99
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Koester, R.
Ang. Chem., 1956 , vol. 68, p. 383 Full Text Show Details
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
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123
Synthesize Find similar Rx-ID: 26616775 Find similar reactions
in ammonia
NH3 (liquid);
Schaeffer, G. W.; Adams, M. D.; Koenig, F. J.
Journal of the American Chemical Society, 1956 , vol. 78, p. 725 - 728 Full Text View citing articles Show Details
in ammonia
NH3 (liquid);
Gmelin Handbook: Na: SVol.3, 1.5.5, page 947 - 953 Full Text Show Details
A
B
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124
Synthesize Find similar Rx-ID: 26091337 Find similar reactions
With sodium amalgam
by-products higher condensed Na-borhydride;
Stridde, G. E.
Diss. Rensselaer Polytechn. Inst. Troy, N. Y., 1955, S. 16 Full Text Show Details
Stridde, G. E.
N.S.A., MCC-1023-TR-136 (1955) 16 1955 , vol. 9, p. 7261 Full Text Show Details
With sodium amalgam
Stridde, G. E.
Diss. Rensselaer Polytechn. Inst. 1955, S. 16 Full Text Show Details
Stridde, G. E.
N.S.A., MCC-1023-TR-136 (1955) 16 1955 , vol. 9, p. 7261 Full Text Show Details
With Na-amalgam
Gmelin Handbook: Na: SVol.3, 3.6.2, page 1223 - 1233 Full Text Show Details
Hide Details
With Na-amalgam by-products higher condensed Na-borhydride;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
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125
Synthesize Find similar Rx-ID: 26075934 Find similar reactions
B: 60%
in neat (no solvent) on trituration at 330-350°C for 20-48h;;
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Gaylord, N. G.
Journal of the American Chemical Society, 1953 , vol. 75, p. 186 - 190 Full Text Show Details
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; Full Text Show Details
Gaylord, N. G.
Reduction with Complex Metal Hydrides, New York-London 1956, S. 15 Full Text Show Details
B: 60%
in neat (no solvent) on trituration at 330-350°C for 20-48h;;
Gmelin Handbook: Na: SVol.2, 90, page 801 - 803 Full Text Show Details
heating at 330 - 350°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Hide Details
126
heating at 330 - 350°C;
Gmelin Handbook: Na: SVol.3, 3.9.1, page 1262 - 1270 Full Text Show Details
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Rx-ID: 26088881 Find similar reactions
byproducts: Na(B(OC2H5)4); disproportionation;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
byproducts: Na(B(OC2H5)4); disproportionation;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
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127
Synthesize Find similar Rx-ID: 26088900 Find similar reactions
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A: <=85
exclusion of air, above -80°C;
Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Hoekstra, H. R.
N.S.A., The Preparation and Properties of Alkali Metal Borohydrides, AECD-2144 (1947) 1/45 1948 , vol. 1, p. 756 Full Text Show Details
over -80°C;
Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Hoekstra, H. R.
N.S.A., AECD-2144 (1947) 17 1948 , vol. 1, p. 756 Full Text Show Details
over -80°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
Hide Details
A: <=85
exclusion of air, above -80°C;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
128
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Rx-ID: 26088901 Find similar reactions
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Synthesize Find similar
78%
in neat (no solvent) heating to 250-270°C, excess NaH;;
Gmelin Handbook: Na: SVol.1, 61, page 259 - 261 Full Text Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; C. A., 1951 , p. 4007 Full Text Show Details
66%
in neat (no solvent) molar ratio NaH:NaB(OCH3)4=4:1, 250.C;; 91percent NaBH4;;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.; Sheft, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 186 - 190 Full Text View citing articles Show Details
66%
in neat (no solvent) molar ratio NaH:NaB(OCH3)4=4:1, 250.C;; 91percent NaBH4;;
Gmelin Handbook: Na: SVol.2, 92, page 805 - 807 Full Text Show Details
A
B
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Synthesize Find similar
129
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Synthesize Find similar
Rx-ID: 26088902 Find similar reactions
A: <=78
excess of NaH, 250 - 270°C; separated with isopropyl amine;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
250-270°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
A: <=78
excess of NaH, 250 - 270°C; separated with isopropyl amine;
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
Hide Details
250-270°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A: <=78
excess of NaH, 250 - 270°C; separated with isopropyl amine;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
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Synthesize Find similar
130
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Synthesize Find similar
Rx-ID: 26091428 Find similar reactions
ambient temp., exothermic reaction;
Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Hoekstra, H. R.
N.S.A., The Preparation and Properties of Alkali Metal Borohydrides, AECD-2144 (1947) S. 16 1948 , vol. 1, p. 756 Full Text Show Details
Schlesinger, H. I.; Hoekstra, H. R.; Brown, H. C.
115th Meeting Am. Chem. Soc., 1949, Abstr. of Papers, S. 9-1O Full Text Show Details
ambient temp., exothermic reaction;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
131
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Synthesize Find similar
Rx-ID: 26091638 Find similar reactions
byproducts: Na(B(OC4H9)4); disproportionation;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
byproducts: Na(B(OC4H9)4); disproportionation;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
132
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Rx-ID: 26101906 Find similar reactions
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Synthesize Find similar
78%
in neat (no solvent) molar ratio NaH:NaBH(OCH3)3=3:1, 250-270°C;;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.; Sheft, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 186 - 190 Full Text View citing articles Show Details
78%
in neat (no solvent) heating to 250-270°C, excess NaH;;
Gmelin Handbook: Na: SVol.1, 61, page 259 - 261 Full Text Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; C. A., 1951 , p. 4007 Full Text Show Details
78%
in neat (no solvent) molar ratio NaH:NaBH(OCH3)3=3:1, 250-270°C;;
Gmelin Handbook: Na: SVol.2, 92, page 805 - 807 Full Text Show Details
Hide Details
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.; Hoekstra, H. R.; Rapp, L. R.
Journal of the American Chemical Society, 1953 , vol. 75, p. 199 - 204 Full Text View citing articles Show Details
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
Gmelin Handbook: B: B-Verb.8, 3.2.1, page 53 - 65 Full Text Show Details
A
B
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Synthesize Find similar
133
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Synthesize Find similar
Rx-ID: 26101907 Find similar reactions
A: <=78
excess of NaH, 250 - 270°C; separated with isopropyl amine;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
250-270°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; C.A., 1951 , p. 4007 Full Text Show Details
A: <=78
excess of NaH, 250 - 270°C; separated with isopropyl amine;
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
Hide Details
250-270°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
Sodium Trimethoxy Borohydride, Bull. 504-C Full Text Show Details
A: <=78
excess of NaH, 250 - 270°C; separated with isopropyl amine;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
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Synthesize Find similar
134
Synthesize Find similar Rx-ID: 26101922 Find similar reactions
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molar ratio of NaH : B(OCH3)3 = 4 : 1, at 225 - 275°C, in low-pressure autoclave; extraction with NH3 (liquid) or isopropyl amine;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Hoekstra, H. R.; Brown, H. C.
115th Meeting Am. Chem. Soc., 1949, Abstr. of Papers, S. 9-1O Full Text Show Details
molar ratio of NaH : B(OCH3)3 = 4 : 1, at 225 - 275°C, in low-pressure autoclave; extraction with NH3 (liquid) or isopropyl amine;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
135
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26101925 Find similar reactions
Synthesize Find similar
Synthesize Find similar
molar ratio of NaH : B(OCH3)3 = 4 : 1, at 225 - 275°C, in low-pressure autoclave;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Hoekstra, H. R.; Brown, H. C.
115th Meeting Am. Chem. Soc., 1949, Abstr. of Papers, S. 9-1O Full Text Show Details
molar ratio of NaH : B(OCH3)3 = 4 : 1, at 225 - 275°C, in low-pressure autoclave;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
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Synthesize Find similar
136
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26101938 Find similar reactions
molar ratio of NaH : B(OCH3)3 = 4 : 1, at 225 - 275°C, in low-pressure autoclave;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Hoekstra, H. R.; Brown, H. C.
115th Meeting Am. Chem. Soc., 1949, Abstr. of Papers, S. 9-1O Full Text Show Details
molar ratio of NaH : B(OCH3)3 = 4 : 1, at 225 - 275°C, in low-pressure autoclave;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
137
B
C
Synthesize Find similar Rx-ID: 26154035 Find similar reactions
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Synthesize Find similar
Synthesize Find similar
byproducts: (CH3)2BH; equilibrium reaction, 230°C, disproportionation;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Hoekstra, H. R.; Brown, H. C.
115th Meeting Am. Chem. Soc., 1949, Abstr. of Papers, S. 9-1O Full Text Show Details
byproducts: (CH3)2BH; equilibrium reaction, 230°C, disproportionation;
Brown, H. C.; Schlesinger, H. I.; Sheet, I.; Ritter, D. M.
Journal of the American Chemical Society, 1953 , vol. 75, p. 192 - 195 Full Text View citing articles Show Details
byproducts: (CH3)2BH; equilibrium reaction, 230°C, disproportionation;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
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Synthesize Find similar
138
Synthesize Find similar Rx-ID: 26375060 Find similar reactions
250°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
250°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A
B
C
139
Synthesize Find similar Rx-ID: 26375062 Find similar reactions
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Synthesize Find similar
Synthesize Find similar
240°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
240°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
140
Synthesize Find similar Rx-ID: 26384558 Find similar reactions
250°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
250°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
250°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
A
141
B
C
D
Synthesize Find similar Rx-ID: 26461269 Find similar reactions
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Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
230°C;
Schlesinger, H. I.; Brown, H. C.; Finholt, A. E.
Journal of the American Chemical Society, 1953 , vol. 75, p. 205 - 209 Full Text View citing articles Show Details
Schlesinger, H. I.; Hoekstra, H. R.; Brown, H. C.
115th Meeting Am. Chem. Soc., 1949, Abstr. of Papers, S.9-0 Full Text Show Details
230°C;
Gmelin Handbook: Na: SVol.3, 3.7, page 1233 - 1245 Full Text Show Details
142
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Rx-ID: 26101893 Find similar reactions
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85-90
in diethyl ether
0.05mol BF3*O(C2H5)2, 0.33mol NaH, abs. ether, at 125°C in a closed tube;;
Wittig, G.; Hornberger, P.
Liebigs Annalen der Chemie, 1952 , vol. 577, p. 11 - 25 Full Text Show Details
85-90
in diethyl ether
in abs. ether, at 125°C, in bomb-tube;
Wittig, G.; Hornberger, P.
Liebigs Annalen der Chemie, 1952 , vol. 577, p. 11 - 25 Full Text Show Details
85-90
in diethyl ether
in abs. ether, at 125°C, in bomb-tube;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Hide Details
85-90
Gmelin Handbook: Na: SVol.2, 90, page 801 - 803 Full Text Show Details
in diethyl ether
0.05mol BF3*O(C2H5)2, 0.33mol NaH, abs. ether, at 125°C in a closed tube;; A
B
143
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Synthesize Find similar
Rx-ID: 26088049 Find similar reactions
Synthesize Find similar
Synthesize Find similar
in neat (no solvent) at 110°C;;
Gmelin Handbook: Na: SVol.2, 92, page 805 - 807 Full Text Show Details
in neat (no solvent) at 110°C;;
Burg, A. B.; Randolph, C. L.
Journal of the American Chemical Society, 1951 , vol. 73, p. 953 - 957 Full Text View citing articles Show Details
A
B
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Synthesize Find similar
144
Synthesize Find similar Rx-ID: 26101855 Find similar reactions
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in neat (no solvent) byproducts: Na-hydrido fluoroborates; at 150-200°C;;
Bergmann, R.
Diss. Goettingen 1950, S. 11 Full Text Show Details
excess of NaH, 180 - 190°C;
Goubeau, J.; Bergmann, R.
Zeitschrift fuer Anorganische und Allgemeine Chemie, 1950 , vol. 163, p. 69 - 81 Full Text Show Details
excess of NaH, 180 - 190°C;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Hide Details
in neat (no solvent) byproducts: Na-hydrido fluoroborates; at 150-200°C;;
Gmelin Handbook: Na: SVol.2, 90, page 801 - 803 Full Text Show Details
145
Synthesize Find similar
Rx-ID: 26101926 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; C. A., 1951 , p. 4007 Full Text Show Details
in neat (no solvent) molar ratio NaH: B(OC4H9)3=4:1, at 225-275°C in an autoclave, extractn. with liquid NH3 or isopropylamine;; high purity;;
146
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Rx-ID: 26121841 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259 Full Text Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; C. A., 1951 , p. 4007 Full Text Show Details
in neat (no solvent) molar ratio NaH: B(OC4H9)3=4:1, at 225-275°C in an autoclave, extractn. with liquid NH3 or isopropylamine;; high purity;;
147
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Rx-ID: 26121879 Find similar reactions
in neat (no solvent)
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Gmelin Handbook: Na: SVol.1, 60, page 257 - 259
byproducts: NaOC2H5; molar ratio NaH: B(OC2H5)3=4:1, at 225-275°C in an autoclave, extractn. with liquid NH3 or isopropylamine;; high purity;;
Full Text Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2534533 , 1950 ; C. A., 1951 , p. 4007 Full Text Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
148
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26088898 Find similar reactions
Schlesinger, H. I.; Brown, H. C.
Patent: US2461661/3 , 1949 ; C.A., 1949 , p. 4684 Full Text Show Details
Gmelin Handbook: B: SVol.1, 4.1.5, page 112 - 115 Full Text Show Details
149
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Synthesize Find similar
Rx-ID: 26091336 Find similar reactions
With sodium amalgam
X-ray;
Kasper, J. S.; McCarty, L. V.; Newkirk, A. E.
Journal of the American Chemical Society, 1949 , vol. 71, p. 2583 Full Text View citing articles Show Details
With sodium amalgam
shaking many hours;
Kasper, J. S.; McCarty, L. V.; Newkirk, A. E.
Journal of the American Chemical Society, 1949 , vol. 71, p. 2583 Full Text View citing articles Show Details
With sodium amalgam
ambient temp.;
Stock, A.; Laudenklos, H.
Zeitschrift fuer Anorganische und Allgemeine Chemie, 1936 , vol. 228, p. 178 - 192 Full Text Show Details
Gmelin Handbook: B: B-Verb.8, 1.1, page 1 - 2 Full Text Show Details
Stock, A.
Hydrides of Boron and Silicon, Cornell University Press, Ithaca - New York - London - Oxford 1933, p.138 Full Text Show Details
Stock, A.
Hydrides of Boron and Silicon, Cornell University Press, Ithaca - New York - London - Oxford 1933, pp. 141/9 Full Text Show Details
Hide Details
With sodium amalgame X-ray;
Gmelin Handbook: B: SVol.1, 4.1.5, page 112 - 115 Full Text Show Details
With Na-amalgam shaking many hours;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
C
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Synthesize Find similar
Synthesize Find similar
150
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26091408 Find similar reactions
Schlesinger, H. I.; Brown, H. C.
Patent: US2461661/3 , 1949 ; C.A., 1949 , p. 4684 Full Text Show Details
Gmelin Handbook: B: SVol.1, 4.1.5, page 112 - 115 Full Text Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
151
Synthesize Find similar Rx-ID: 26091426 Find similar reactions
Synthesize Find similar
Schlesinger, H. I.; Brown, H. C.
Patent: US2461661/3 , 1949 ; C.A., 1949 , p. 4684 Full Text Show Details
Gmelin Handbook: B: SVol.1, 4.1.5, page 112 - 115 Full Text Show Details
152
Synthesize Find similar
Rx-ID: 26091427 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Gmelin Handbook: Na: SVol.1, 61, page 259 - 261 Full Text Show Details
Schlesinger, H. I.; Brown, H. C.
Patent: US2561662 , 1949 ; C. A., 1949 , p. 4684 Full Text Show Details
in neat (no solvent) byproducts: B(OCH3)3; at ambient temp., fast react., exothermic react.;;
153
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Rx-ID: 26091407 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Stock, A.; Laudenklos, H.
Zeitschrift fuer Anorganische und Allgemeine Chemie, 1936 , vol. 228, p. 178 - 192 Full Text Show Details
Gmelin Handbook: B: B-Verb.8, 1.1, page 1 - 2 Full Text Show Details
Stock, A.
Hydrides of Boron and Silicon, Cornell University Press, Ithaca - New York - London - Oxford 1933, p.138 Full Text Show Details
Stock, A.
Hydrides of Boron and Silicon, Cornell University Press, Ithaca - New York - London - Oxford 1933, pp. 141/9 Full Text Show Details
ambient temp.;
154
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Synthesize Find similar
Synthesize Find similar
Rx-ID: 26070296 Find similar reactions
Schrauzer, G.
Diss. Muenchen 1956, S. 130 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 52 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
in tetrahydrofuran
155
Synthesize Find similar
Rx-ID: 26070311 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Schrauzer, G.
Diss. Muenchen 1956, S. 130 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 52 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
in tetrahydrofuran
A
B
Synthesize Find similar
Synthesize Find similar
156
Synthesize Find similar Rx-ID: 26101942 Find similar reactions
A: 86-94
Synthesize Find similar
NaH heating in N2 atmoshpere to 220°C, addn. of B(OCH3) by stirring dropwisse (20-40 min) at 230-270°C, stirring 1 h, cooling, yield depending on quality of NaH; extraction with dry isopropyl amine or NH3, filtering, solvent evapn., purity 90-96 percent;
A
B
Gmelin Handbook: B: B-Verb.8, 1.2, page 2 - 5 Full Text Show Details
Becher, H. J.
in: G. Brauer, Handbuch der Praeparativen Anorganischen Chemie, 2. Edn., Vol. 1, Ferdinand Enke, Stuttgart 1960, pp.689/91 Full Text Show Details
157
Synthesize Find similar
Synthesize Find similar
Rx-ID: 26121919 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Gmelin Handbook: B: B-Verb.8, 1.2, page 2 - 5 Full Text Show Details
Hinkley, A. A.
in: Kirk-Othmer, Encyclopedia of Chemical Technology, 2. Edn., Vol. 11, Interscience Publishers, New York London - Sidney 1966, pp. 210/7 Full Text Show Details
in water; mineral oil
Na suspended in mineral oil with water; yield depending on temp.; extraction with i-propylamine, drying, purity 98 percent;
158
Synthesize Find similar
Rx-ID: 26161996 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Schrauzer, G.
Diss. Muenchen 1956, S. 130 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 52 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
in tetrahydrofuran
A
B
Synthesize
Synthesize
159
Synthesize
Find similar Rx-ID: 26165427 Find similar reactions
Find similar
Find similar
in tetrahydrofuran
ambient temp.;
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
ambient temp.;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
160
Synthesize Find similar Rx-ID: 26165865 Find similar reactions
in tetrahydrofuran
ambient temp.;
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
ambient temp.;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
161
Synthesize Find similar Rx-ID: 26167020 Find similar reactions
in tetrahydrofuran
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
thermic decompn.;
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Hide Details
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
thermic decompn.;
A
B
Synthesize Find similar
Synthesize Find similar
162
Synthesize Find similar Rx-ID: 26167022 Find similar reactions
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
thermic decompn.;
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Hide Details
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
thermic decompn.;
A
B
163
Synthesize Find similar Rx-ID: 26167023 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
thermic decompn.;
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
thermic decompn.;
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
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Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
in tetrahydrofuran
A
B
Synthesize Find similar
Synthesize Find similar
164
Synthesize Find similar Rx-ID: 26167025 Find similar reactions
in tetrahydrofuran
thermic decompn.;
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Hide Details
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
thermic decompn.;
A
B
Synthesize Find similar
Synthesize Find similar
165
Synthesize Find similar Rx-ID: 26167103 Find similar reactions
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
thermic decompn.;
Schrauzer, G.
Diss. Muenchen 1956, S. 119/20 Full Text Show Details
Schrauzer, G.
Diss. Muenchen 1956, S. 46/7 Full Text Show Details
in tetrahydrofuran
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
Hide Details
Gmelin Handbook: Na: SVol.3, 3.6.1, page 1212 - 1222 Full Text Show Details
thermic decompn.;
A
166
B
Synthesize Find similar Rx-ID: 26484225 Find similar reactions
Synthesize Find similar
Synthesize Find similar
With NaC2H in ammonia
byproducts: C2H4;
Shore, S. G.; Hickam, C. W.
Abstr. Papers 141st Meeting Am. Chem. Soc., Washington, D.C., 1962, S. 5 M Full Text Show Details
With NaC2H in ammonia
byproducts: C2H4; NH3 (liquid);
Gmelin Handbook: B: B-Verb.4, 4.2.1, page 92 - 95 Full Text Show Details