Cyclohexanone by Asch

Reaxys

PubChem

eMolecules

Reactions (1470)

Yield

Substances (2)

Citations (3478)

Conditions

References A

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1189 Synthesize Find similar

Rx-ID: 1073172 Find similar reactions

Bigler,P.; Neuenschwander,M.

Helvetica Chimica Acta, 1978 , vol. 61, p. 2165 - 2175 Full Text View citing articles Show Details

T=20°C; Equilibrium constant;

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1190 Synthesize Find similar

in cyclohexane; cyclohexene

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Rx-ID: 25339687 Find similar reactions

Rhone - Poulenc Industries

Patent: US4093636 A1, 1978 ; Title/Abstract Full Text Show Details

34:EXAMPLE 34

EXAMPLE 34 1.4 Mols of cyclohexene, 0.5 mol of cyclohexane and 0.4 millimol of trichloro-butyl-tin are introduced into a 200 cm3 three-necked glass flask which is kept under an inert atmosphere and surmounted by a

reflux condenser. The mixture is heated to the reflux temperature (82° C.), then 0.08 mol of CHHPO is introduced and this temperature is maintained for 45 minutes. Degree of conversion of the hydroperoxide: 92.6percent. Yield of epoxide: 90.7percent (yield relative to the hydroperoxide converted). Yield of cyclohexanol: 96.5percent. Yield of cyclohexanone: 2percent. A

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1191 Synthesize Find similar Rx-ID: 26757682 Find similar reactions

A: 71% C: 29%

byproducts: CO2; 52 percent decompn. at 150°C/0.8 Torr for 8 h;

Didier, P.; Pommier, J. C.

Journal of Organometallic Chemistry, 1978 , vol. 150, p. 203 - 214 Full Text View citing articles Show Details

A: 71% C: 29%

byproducts: CO2; 52 percent decompn. at 150°C/0.8 Torr for 8 h;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

A: 66% C: 34%

byproducts: CO2; 52 percent decompn. at 200°C/8 Torr for 4.5 h;

Didier, P.; Pommier, J. C.

Journal of Organometallic Chemistry, 1978 , vol. 150, p. 203 - 214 Full Text View citing articles Show Details

Hide Details A: 66% C: 34%

byproducts: CO2; 52 percent decompn. at 200°C/8 Torr for 4.5 h;

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Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

1192

Rx-ID: 25212465 Find similar reactions

UBE Industries, Ltd.

Patent: US4010206 A1, 1977 ;

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Title/Abstract Full Text Show Details

8:EXAMPLE 8

EXAMPLE 8 The same autoclave as used in Example 1 was used to prepare a solution from 4.60g (26.4 m mole) of p-cyclohexyltoluene and 17g of benzene. After closing the autoclave, hydrogen bromide was introduced into the solution so that the concentration thereof in the solution was adjusted to 0.15 mole/l. Thereafter, air was introduced into the solution under a pressure of 15 atmospheres for 20 minutes while stirring and maintaining the oxidation mixture at a temperature of 55° C. It was determined that 2.00g (11.4 m mole) of p-cyclohexyltoluene were consumed and p-cresol and cyclohexanone were respectively obtained in amount of 0.97g (8.98 m mole, yield percentage=34.0, selectivity percentage=79.0) and 0.84g (8.53 m mole, yield percentage=32.3 and selectivity percentage=75.0). A

1193

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Rx-ID: 25265759 Find similar reactions

UBE Industries, Ltd.

Patent: US4010206 A1, 1977 ;

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Title/Abstract Full Text Show Details

1:EXAMPLE 1

The azeotropic mixture obtained above was mixed with 1,4-butanediol in a weight of five times that the azeotropic mixture. The mixture was first distilled at a temperature of 27° C under a reduced pressure of 5 mmHg to separate cyclohexanone and then distilled at a temperature of 62° C under the same reduced pressure as above, to separate phenol. The resultant phenol and cyclohexanone were obtained in amounts of 15.1 m mole (yield percentage=52.2 and selectivity percentage=97.1) and 14.0 m mole (yield percentage=48.4 and selectivity percentage=91.1). A

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1194

Rx-ID: 25210725 Find similar reactions

BP Chemicals (U.K.) Limited

Patent: US3947406 A1, 1976 ;

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Title/Abstract Full Text Show Details

39:EXAMPLE 39

Distillation gave cyclohexanone and dihydroisophorone (9.0 g.), an intermediate fraction (3.2 g.), b.p. below 100°C/0.7 mm., Hg., a fraction (8.1 g.), b.p. 110° - 114° 10.7 mm. of 3,3,5'-trimethyl-1,1'-peroxydicyclohexylamine (peroxide equivalent, 234; perchloric acid equivalent, 245; and residue (1.5 g.). A

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1195

Rx-ID: 25212157 Find similar reactions

BP Chemicals International Limited

Patent: US3983142 A1, 1976 ;

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Title/Abstract Full Text Show Details

19:EXAMPLE 19

EXAMPLE 19 The same reactants were used as in Example 18 with the addition of magnesium sulphate monohydrate (1.5 g) to the refluxing solution. Heating was continued for 51/4 hours. Treatment of the reaction mixture as in Example 18 gave a cyclohexanone fraction (2.8 g), a caprolactam fraction (4.1 g containing 81percent lactam by I.R.), and residue (0.2 g). Further caprolactam (0.2 g) was obtained by acidification of the aqueous phase followed by extraction with chloroform.

1196 Synthesize Find similar

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Rx-ID: 25268090 Find similar reactions

BP Chemicals (U.K.) Limited

Patent: US3947406 A1, 1976 ;

in methanol

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Title/Abstract Full Text Show Details

40:EXAMPLE 40

EXAMPLE 40 1-Aminocyclohexyl hydroperoxide (13.1 g.), butyraldehyde (7.2 g.), methanol (25 cc.) and ammonia acetate (1.0 g.) were mixed and stored at 0°C overnight. Working up as in Example 39 gave cyclohexanone and butyraldehyde, and a product (8.4 g.), b.p. 89°/0.3 mm. (peroxide equivalent, 204; pechloric acid equivalent, 206; which was identified as SPC37

1197 Synthesize Find similar

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Rx-ID: 26412371 Find similar reactions

76%

With NO{BF4} in dichloromethane

for 1 h at 20°C;

Olah, G. A.; Ho, T. L.

Synthesis, 1976 , p. 609 - 610 Full Text Show Details

76%

With NO{BF4} in dichloromethane

for 1 h at 20°C;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.6, page 64 - 69 Full Text Show Details

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1198 Synthesize Find similar

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Rx-ID: 26412373 Find similar reactions

A: 10% B: 75% D: 70% E: 20%

Irradiation (UV/VIS); equimolar ratio of educts; UV irradn., for 14 h (or 15 h) at 70 (or 80)°C;

Pommier et al.

Journal of Organometallic Chemistry, 1971 , vol. 31, p. C59 Full Text View citing articles Show Details

Pommier, J. C.; Chevolleau, D.

Journal of Organometallic Chemistry, 1974 , vol. 74, p. 405 - 416 Full Text View citing articles Show Details

A: 10% B: 75% D: 70% E: 20%

Irradiation (UV/VIS); equimolar ratio of educts; UV irradn., for 14 h (or 15 h) at 70 (or 80)°C;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.6, page 64 - 69 Full Text Show Details

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1199 Synthesize Find similar

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Rx-ID: 26712306 Find similar reactions

B: 18%

38percent yield of CHCl3 and CDCl3;

Pommier, J. C.; Chevolleau, D.

D: 14% E: 38%

Journal of Organometallic Chemistry, 1974 , vol. 74, p. 405 - 416 Full Text View citing articles Show Details

B: 18% D: 14% E: 38%

38percent yield of CHCl3 and CDCl3;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.6, page 64 - 69 Full Text Show Details

1200 Synthesize Find similar

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Rx-ID: 26756201 Find similar reactions

77%

decompn. at 150°C for 0.5 h;

Delmond; Pommier

Tetrahedron Letters, 1968 , p. 6147 Full Text View citing articles Show Details

77%

decompn. at 150°C for 0.5 h;

Delmond, Bernard; Pommier, Jean-Claude; Valade, Jacques

Journal of Organometallic Chemistry, 1972 , vol. 35, # 1 p. 91 - 104 Title/Abstract Full Text View citing articles Show Details

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

1201 Synthesize Find similar

77%

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Rx-ID: 26756223 Find similar reactions

Delmond, Bernard; Pommier, Jean-Claude; Valade, Jacques

Journal of Organometallic Chemistry, 1972 , vol. 35, # 1 p. 91 - 104 Title/Abstract Full Text View citing articles Show Details

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.7, page 69 - 97 Full Text Show Details

decompn. at 210°C for 0.5 h;

1202 Synthesize Find similar

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Rx-ID: 4304511 Find similar reactions

With lutidine; water in ethanol

T=125.2 - 175.5°C; Kinetics;

Pfeifer,W.D. et al.

Journal of the American Chemical Society, 1971 , vol. 93, # 6 p. 1513 - 1516 Full Text View citing articles Show Details

1203

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Rx-ID: 26412375 Find similar reactions

B: 43%

Irradiation (UV/VIS); at 80°C;

Pommier et al.

Journal of Organometallic Chemistry, 1971 , vol. 31, p. C59 Full Text View citing articles Show Details

B: 43%

Irradiation (UV/VIS); at 80°C;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.6, page 64 - 69 Full Text Show Details

B: 4%

at 200°C;

Pommier et al.

Journal of Organometallic Chemistry, 1971 , vol. 31, p. C59 Full Text View citing articles Show Details

Hide Details

B: 4%

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.6, page 64 - 69 Full Text Show Details

at 200°C;

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1204 Synthesize Find similar

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Rx-ID: 26412377 Find similar reactions

B: 45%

Irradiation (UV/VIS); by UV irradn. at 80°C; no reaction at 200°C without irradiation;

Pommier et al.

Journal of Organometallic Chemistry, 1971 , vol. 31, p. C59 Full Text View citing articles Show Details

B: 45%

Irradiation (UV/VIS); by UV irradn. at 80°C; no reaction at 200°C without irradiation;

Gmelin Handbook: Sn: Org.Comp.12, 1.4.1.1.1.5.2.1.6, page 64 - 69 Full Text Show Details

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1205 Synthesize Find similar

Rx-ID: 4301668 Find similar reactions

Wheeler,O.H.

Journal of Organic Chemistry, 1964 , vol. 29, p. 3634 - 3636 Full Text View citing articles Show Details

in ethanol

T=23°C; Equilibrium constant;

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1206 Synthesize Find similar Rx-ID: 714791

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Pudowik; Konowalowa

Zhurnal Obshchei Khimii, 1962 , Zhurnal Obshchei Khimii, 1963 , Full Text Show Details

Pudowik; Konowalowa

Zhurnal Obshchei Khimii, 1957 , Zhurnal Obshchei Khimii, 1963 , Full Text Show Details

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vol. 32, p. 467,469;engl.Ausg.S.460 vol. 33, p. 98;engl.Ausg.S.91 vol. 27, p. 1621; engl. Ausg. S. 1689, 1692 vol. 33, p. 101

1207 Synthesize Find similar

Rx-ID: 1061719 Find similar reactions

With water

T=25 - 50°C; KineticsEquilibrium constant;

Fiarman,I.D.; Gettler,J.D.

Journal of the American Chemical Society, 1962 , vol. 84, p. 961 - 966 Full Text View citing articles Show Details

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1208 Synthesize Find similar

Rx-ID: 1112307 Find similar reactions

With water

T=25 - 50°C; KineticsEquilibrium constant;

Brooks,D.W.; Gettler,J.D.

Journal of Organic Chemistry, 1962 , vol. 27, p. 4469 - 4475 Full Text View citing articles Show Details

1209 Synthesize Find similar

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Schultz

Journal of Organic Chemistry, 1960 , vol. 25, p. 1039,1040 Full Text Show Details

Behandeln des Reaktionsprodukts mit wss. Salzsaeure;

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1210 Synthesize Find similar

Rx-ID: 7441799 Find similar reactions

Rx-ID: 418175 Find similar reactions

Gray; Williams

Transactions of the Faraday Society, 1959 , vol. 55, p. 760,764 Full Text Show Details

Thermodynamic data;

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1211 Synthesize Find similar

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Rx-ID: 598645 Find similar reactions

Kuskow; Newerow

Zhurnal Obshchei Khimii, 1959 , vol. 29, p. 1127; engl. Ausg. S. 1096 Full Text Show Details

T=260°C;

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1212 Synthesize Find similar

Rx-ID: 5720303 Find similar reactions

Nasarow; Sarezkaja

Zhurnal Obshchei Khimii, 1959 , vol. 29, p. 1558,1559 J. Gen. Chem. USSR (Engl. Transl.), 1959 , vol. 29, p. 1532,1533 Full Text Show Details

T=160°C;

1213 Synthesize Find similar

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Rx-ID: 5818056 Find similar reactions

Smidt et al.

Angewandte Chemie, 1959 , vol. 71, p. 176,180,182 Angewandte Chemie, 1962 , vol. 74, p. 93 Full Text Show Details

T=30°C;

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1214 Synthesize Find similar Rx-ID: 6208227 Find similar reactions

T=300°C;

Landa et al.

Collection of Czechoslovak Chemical Communications, 1959 ,

vol. 24, p. 1036,1038,1039 Full Text Show Details

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1215 Synthesize Find similar

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Rx-ID: 6215335 Find similar reactions

Matschinskaja; Barchasch

Zhurnal Obshchei Khimii, 1959 , vol. 29, p. 2786,2789 J. Gen. Chem. USSR (Engl. Transl.), 1959 , vol. 29, p. 2750,2752 Full Text Show Details

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1216 Synthesize Find similar

Rx-ID: 7065969 Find similar reactions

Chang et al.

Wuhan Univ. J. nat. Sci.Chem.Abstr., 1959 , # 5 p. 57 Wuhan Univ. J. nat. Sci.Chem.Abstr., 1960 , p. 5509 Full Text Show Details

T=80°C; UV-Licht;

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1217 Synthesize Find similar

Rx-ID: 7065970 Find similar reactions

Chang et al.

Wuhan Univ. J. nat. Sci.Chem.Abstr., 1959 , # 5 p. 57 Wuhan Univ. J. nat. Sci.Chem.Abstr., 1960 , p. 5509 Full Text Show Details

T=80°C; UV-Licht;

1218 Synthesize Find similar

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Rx-ID: 8269877 Find similar reactions

Taguchi; Kojima

Journal of the American Chemical Society, 1959 , vol. 81, p. 4318,4321 Full Text Show Details

1219 Synthesize Find similar

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Rx-ID: 8282069 Find similar reactions

Taguchi; Kojima

Journal of the American Chemical Society, 1959 , vol. 81, p. 4318,4321 Full Text Show Details

1220 Synthesize Find similar

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Rx-ID: 8289353 Find similar reactions

Mousseron et al.

Bulletin de la Societe Chimique de France, 1948 , p. 84,88 Full Text Show Details

Taguchi; Kojima

Journal of the American Chemical Society, 1959 , vol. 81, p. 4318,4321 Full Text Show Details

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1221 Synthesize Find similar

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Rx-ID: 164255 Find similar reactions

Equilibrium constant;

Prelog; Kobelt

Helvetica Chimica Acta, 1949 , vol. 32, p. 1187,1191 Full Text Show Details

Ruzicka; Plattner; Wild

Helvetica Chimica Acta, 1945 , vol. 28, p. 613,615 Full Text Show Details

T=25°C; Equilibrium constant;

Wheeler; Zabicky

Canadian Journal of Chemistry, 1958 , vol. 36, p. 656 Full Text Show Details

El-Abbady

Journal of Organic Chemistry, 1956 , vol. 21, p. 828 Full Text View citing articles Show Details

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1222 Synthesize Find similar Rx-ID: 399717

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Bennett et al.

Journal of the Chemical Society, 1958 , p. 4508,4513 Full Text Show Details

T=495°C; Pyrolysis;

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1223 Synthesize Find similar

Rx-ID: 537923 Find similar reactions

With xylene

Taguchi; Eto

Journal of the American Chemical Society, 1958 , vol. 80, p. 4075,4077 Full Text Show Details

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1224 Synthesize Find similar

Rx-ID: 5589276 Find similar reactions

Goustille; Cordier

Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1958 , vol. 246, p. 3350 Full Text View citing articles Show Details

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1225 Synthesize Find similar

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Rx-ID: 5687525 Find similar reactions

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Newman; Harper

Journal of the American Chemical Society, 1958 , vol. 80, p. 6350,6353 Full Text View citing articles Show Details

T=30°C; Equilibrium constant;

1226 Synthesize Find similar

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T=160 - 180°C; Rate constant;

Rx-ID: 5818049 Find similar reactions

Thonon; Jungers

Bulletin des Societes Chimiques Belges, 1950 , vol. 59, p. 604,606

Full Text Show Details

Claes; Jungers

Bulletin de la Societe Chimique de France, 1958 , p. 1167,1169,1172 Full Text Show Details

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1227 Synthesize Find similar

Rx-ID: 6208381 Find similar reactions

Thonon; Jungers

Bulletin des Societes Chimiques Belges, 1950 , vol. 59, p. 604,606 Full Text Show Details

Claes; Jungers

Bulletin de la Societe Chimique de France, 1958 , p. 1167,1169,1172 Full Text Show Details

T=160 - 180°C; Rate constant;

1228 Synthesize Find similar

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Rx-ID: 6213947 Find similar reactions

Kuhn; Haas

Justus Liebigs Annalen der Chemie, 1958 , vol. 611, p. 57,63 Full Text Show Details

Hydrogenation;

1229 Synthesize Find similar

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Rx-ID: 6680215 Find similar reactions

Richter; Besta

Chem. PrumyslChem.Abstr., 1958 , vol. 8, p. 62 Chem. PrumyslChem.Abstr., 1958 , p. 15444 Full Text Show Details

in Abhaengigkeit von der Zeit, der Temperatur und der KOH-Konzentration;

1230 Synthesize Find similar

Hydrogenation;

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Rx-ID: 6680216 Find similar reactions

Kuhn; Haas

Justus Liebigs Annalen der Chemie, 1958 , vol. 611, p. 57,63 Full Text Show Details

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1231 Synthesize Find similar

Rx-ID: 6680222 Find similar reactions

Richter; Ruzicka

Chem. PrumyslChem.Abstr., 1958 , vol. 8, p. 116 Chem. PrumyslChem.Abstr., 1959 , p. 5156 Full Text Show Details

T=300 - 400°C; P=20 - 760 Torr;

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1232 Synthesize Find similar

Rx-ID: 7054809 Find similar reactions

Wheeler; Mateos

Canadian Journal of Chemistry, 1958 , vol. 36, p. 712,713 Full Text Show Details

T=25°C; Equilibrium constant;

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1233 Synthesize Find similar

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Rx-ID: 7054811 Find similar reactions

Kharasch; Sosnovsky

Journal of Organic Chemistry, 1958 , vol. 23, p. 1322,1324 Full Text Show Details

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1234 Synthesize Find similar

Rx-ID: 7065976 Find similar reactions

Denisow

Zhurnal Fizicheskoi Khimii, 1958 , vol. 32, p. 1269 Chem.Abstr., 1959 , p. 1904 Full Text Show Details

T=110°C; Kinetics;

1235 Synthesize Find similar

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Rx-ID: 7065977 Find similar reactions

Denisow

Zhurnal Fizicheskoi Khimii, 1958 , vol. 32, p. 1269 Chem.Abstr., 1959 , p. 1904 Full Text Show Details

T=110°C; Kinetics;

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1236 Synthesize Find similar

Rx-ID: 7065978 Find similar reactions

Denisow

Zhurnal Fizicheskoi Khimii, 1958 , vol. 32, p. 1269 Chem.Abstr., 1959 , p. 1904 Full Text Show Details

T=110°C; Kinetics;

1237 Synthesize Find similar

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Rx-ID: 8236269 Find similar reactions

Schenck; Schulte-Elte

Justus Liebigs Annalen der Chemie, 1958 , vol. 618, p. 185,191 Full Text View citing articles Show Details

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1238 Synthesize Find similar

Richter; Ruzicka

Chem. PrumyslChem.Abstr., 1958 , vol. 8, p. 116 Chem. PrumyslChem.Abstr., 1959 , p. 5156 Full Text Show Details

T=300 - 400°C; P=20 - 760 Torr;

Rx-ID: 8236278 Find similar reactions

1239

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Rx-ID: 8236287 Find similar reactions

With xylene

T=125°C;

Taguchi; Eto

Journal of the American Chemical Society, 1958 , vol. 80, p. 4075,4077 Full Text Show Details

1240 Synthesize Find similar

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Rx-ID: 8277754 Find similar reactions

T=20 - 40°C; in wss. Loesung vom pH 3; Kinetics;

Blackadder; Hinshelwood

Journal of the Chemical Society, 1958 , p. 2720 Full Text Show Details

T=20 - 40°C; in wss. Loesung vom pH 5; Kinetics;

Blackadder; Hinshelwood

Journal of the Chemical Society, 1958 , p. 2720 Full Text Show Details

1241 Synthesize Find similar Rx-ID: 19223 Find similar reactions

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Stuckwisch et al.

Journal of Organic Chemistry, 1957 , vol. 22, p. 1678 Full Text View citing articles Show Details

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1242 Synthesize Find similar Rx-ID: 96646 Find similar reactions

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Urbanski et al.

Roczniki Chemii, 1957 , vol. 31, p. 93,96 Chem.Abstr., 1957 , p. 14717 Full Text Show Details

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1243 Synthesize Find similar

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Rx-ID: 96647 Find similar reactions

Urbanski et al.

Roczniki Chemii, 1957 , vol. 31, p. 93,96 Chem.Abstr., 1957 , p. 14717 Full Text Show Details

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1244 Synthesize Find similar

Rx-ID: 819075 Find similar reactions

Allan et al.

Journal of the Chemical Society, 1957 , p. 4700,4705 Full Text Show Details

T=500°C;

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1245 Synthesize Find similar Rx-ID: 837570 Find similar reactions

Allan et al.

Journal of the Chemical Society, 1957 , p. 4700,4705 Full Text Show Details

T=500°C; Pyrolysis;

1246 Synthesize Find similar

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T=0°C; Rate constant;

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Rx-ID: 5818045 Find similar reactions

Hawthorne

Journal of the American Chemical Society, 1957 , vol. 79, p. 2510,2512 Full Text Show Details

1247 Synthesize Find similar

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Rx-ID: 5818051 Find similar reactions

T=330°C;

Holst

Zeitschrift fuer Physikalische Chemie (Leipzig), 1939 , vol. <A> 183, p. 423,428 Anm. 1 Full Text Show Details

T=280°C;

Treibs; Schmidt

Chemische Berichte, 1927 , vol. 60, p. 2339 Full Text Show Details

Belozerkowsski

Plasticheskie Massy, 1935 , # 3 p. 12 Chem. Zentralbl., 1936 , vol. 107, # I p. 175 Full Text Show Details

T=196 - 236°C; Rate constant;

Balandin; Teteni

Doklady Akademii Nauk SSSR, 1957 , vol. 113, p. 1090 Doklady Physical Chemistry, 112-117<1957>235 Full Text Show Details

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1248 Synthesize Find similar

Rx-ID: 7054807 Find similar reactions

Denisow; Emanuel'

Zhurnal Fizicheskoi Khimii, 1957 , vol. 31, p. 1266 Chem.Abstr., 1958 , p. 3485 Full Text Show Details

T=110°C; sowie bei 140grad; auch nach Zusatz von Kobalt(II)-stearat; Kinetics;

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1249 Synthesize Find similar

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Rx-ID: 7054813 Find similar reactions

Gardner et al.

Journal of Organic Chemistry, 1957 , vol. 22, p. 1206,1209 Full Text View citing articles Show Details

Knight; Cram

Journal of the American Chemical Society, 1951 , vol. 73, p. 4136 Full Text View citing articles Show Details

1250 Synthesize Find similar

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Rx-ID: 7065975 Find similar reactions

Inoue

Bl. Tokyo Inst. Technol.Chem.Abstr., 1957 , vol. <A>, p. 103 Bl. Tokyo Inst. Technol.Chem.Abstr., 1959 , p. 4974 Full Text Show Details

stille elektrische Entladungen;

1251 Synthesize Find similar Rx-ID: 7441800 Find similar reactions

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Hawthorne; Strahm

Journal of the American Chemical Society, 1957 , vol. 79, p. 2515,2517 Full Text Show Details

T=50°C; Rate constant;

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1252 Synthesize Find similar Rx-ID: 7444909 Find similar reactions

Ewentowa et al.

Vestnik Moskovskogo Universiteta, 1957 , vol. 12, # 3 p. 175,178 Chem.Abstr., 1958 , p. 6211 Full Text Show Details

T=175°C;

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1253 Synthesize Find similar

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Rx-ID: 57260 Find similar reactions

Rondestvedt; Rowley

Journal of the American Chemical Society, 1956 , vol. 78, p. 3804,3805 Full Text Show Details

T=65°C; sowie bei 75grad; Rate constant;

1254 Synthesize Find similar

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Rx-ID: 675982 Find similar reactions

Tilitschenko; Chartschenko

Doklady Akademii Nauk SSSR, 1956 , vol. 110, p. 226,228, 229 Doklady Chemistry, 106-111 <1956> 561, 562 Full Text View citing articles Show Details

T=245°C;

1255 Synthesize Find similar

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Rx-ID: 712903 Find similar reactions

Hydrogenation.Leiten des erhaltenen Amin-Gemisches mit Wasserstoff und H2O ueber einen KupfersilicatKatalysator bei 250grad;

BASF

Patent: US2879295 , 1956 ; Full Text Show Details

1256 Synthesize Find similar

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Rx-ID: 7054799 Find similar reactions

Pritzkow; Mueller

Chemische Berichte, 1956 , vol. 89, p. 2318,2319 Full Text Show Details

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1257 Synthesize Find similar

1258

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Rx-ID: 7065967 Find similar reactions

Pritzkow; Mueller

Chemische Berichte, 1956 , vol. 89, p. 2318,2319 Full Text Show Details

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Rx-ID: 7441798 Find similar reactions

Boyer et al.

Journal of the American Chemical Society, 1956 , vol. 78, p. 325 Full Text View citing articles Show Details

1259 Synthesize Find similar

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Rx-ID: 8236281 Find similar reactions

Hayes et al.

Journal of the American Chemical Society, 1956 , vol. 78, p. 2527 Full Text View citing articles Show Details

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1260 Synthesize Find similar

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Rx-ID: 346832 Find similar reactions

Zymalkowski

Archiv der Pharmazie (Weinheim, Germany), 1955 , vol. 288, p. 162,169 Full Text Show Details

und anschliessenden Hydrieren an Palladium/Bariumsulfat;

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1261 Synthesize Find similar

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Rx-ID: 629453 Find similar reactions

Zymalkowski

Archiv der Pharmazie (Weinheim, Germany), 1955 , vol. 288, p. 162,169 Full Text Show Details

und anschliessenden Hydrieren an Palladium/Bariumsulfat;

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1262 Synthesize Find similar

Rx-ID: 7065966 Find similar reactions

Ohta; Tezuka

Kogyo Kagaku Zasshi, 1955 , vol. 58, p. 680 Chem.Abstr., 1956 , p. 11255 Full Text Show Details

Ohta; Tezuka

Kogyo Kagaku Zasshi, 1954 , vol. 57, p. 641,723 Chem.Abstr., 1955 , p. 8675,10201 Full Text Show Details

T=120 - 180°C; P=5320 - 18240 Torr;

1263 Synthesize Find similar

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Rx-ID: 7441809 Find similar reactions

Klager

Journal of Organic Chemistry, 1955 , vol. 20, p. 1348 Full Text View citing articles Show Details

Behandeln des Reaktionsprodukts mit wss. Salzsaeure;

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1264 Synthesize Find similar

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Rx-ID: 8236283 Find similar reactions

Taguchi; Kojima

Pharmaceutical Bulletin, 1955 , vol. 3, p. 351,353 Full Text Show Details

Solvolyse;

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1265 Synthesize Find similar

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Rx-ID: 8236284 Find similar reactions

Taguchi; Kojima

Pharmaceutical Bulletin, 1955 , vol. 3, p. 351,353 Full Text Show Details

Solvolyse;

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1266 Synthesize Find similar

Solvolyse;

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Rx-ID: 8236285 Find similar reactions

Taguchi; Kojima

Pharmaceutical Bulletin, 1955 , vol. 3, p. 351,353

Full Text Show Details

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1267 Synthesize Find similar

Rx-ID: 8236286 Find similar reactions

Taguchi; Kojima

Pharmaceutical Bulletin, 1955 , vol. 3, p. 351,353 Full Text Show Details

Solvolyse;

1268 Synthesize Find similar

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Rx-ID: 146484 Find similar reactions

Orazi; Corral

Anales de la Asociacion Quimica Argentina (1921-2001), 1954 , vol. 42, p. 139,145 Full Text Show Details

T=25°C; Rate constant;

1269 Synthesize Find similar

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Rx-ID: 368029 Find similar reactions

Price; Berti

Journal of the American Chemical Society, 1954 , vol. 76, p. 1207,1208 Full Text Show Details

T=230°C;

1270 Synthesize Find similar

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Rx-ID: 5589267 Find similar reactions

T=150 - 250°C; P=51485.6 - 102971 Torr; in Gegenwart eines Hydrierungs-Katalysators;

Olin Mathieson Chem. Corp.

Patent: US2822398 , 1954 ; Full Text Show Details

1271 Synthesize Find similar

Rx-ID: 5589271 Find similar reactions

With sulfur dioxide

in wss. Loesung vom pH 1 -2;

Olin Mathieson Chem. Corp.

Patent: US2795616 , 1954 ; Full Text Show Details

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1272 Synthesize Find similar

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Rx-ID: 5818065 Find similar reactions

Russell

Journal of the American Chemical Society, 1954 , vol. 76, p. 1595 Full Text View citing articles Show Details

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1273 Synthesize Find similar

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Rx-ID: 5818067 Find similar reactions

Pratt; Frazza

Journal of the American Chemical Society, 1954 , vol. 76, p. 6174,6178 Full Text Show Details

1274 Synthesize Find similar

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Behandeln des Reaktionsprodukts mit Natriumhydrogensulfit, Magnesiumhydroxid und Wasser;

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Rx-ID: 7054798 Find similar reactions

Hobbs; Houston

Journal of the American Chemical Society, 1954 , vol. 76, p. 1254 Full Text View citing articles Show Details

1275 Synthesize Find similar

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Rx-ID: 7065968 Find similar reactions

Ewentowa et al.

Vestnik Moskovskogo Universiteta, 1954 , vol. 9, # 6 p. 91 Chem.Abstr., 1955 , p. 12313 Full Text Show Details

T=140°C; fluessiges Isopropylcyclohexan;

1276 Synthesize Find similar Rx-ID: 19217 Find similar reactions

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Grob; Schmid

Helvetica Chimica Acta, 1953 , vol. 36, p. 1763,1769 Full Text Show Details

1277 Synthesize Find similar Rx-ID: 22174 Find similar reactions

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Grob; Schmid

Helvetica Chimica Acta, 1953 , vol. 36, p. 1763,1769 Full Text Show Details

1278 Synthesize Find similar

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Rx-ID: 5818059 Find similar reactions

Ohta et al.

Kogyo Kagaku Zasshi, 1953 , vol. 56, p. 330 Chem.Abstr., 1954 , p. 10415 Full Text Show Details

Ohta et al.

Rep. Gov. chem. ind. Res. Inst. TokyoChem.Abstr., 1953 , vol. 48, p. 181 Rep. Gov. chem. ind. Res. Inst. TokyoChem.Abstr., 1953 , p. 12700 Full Text Show Details

T=275 - 350°C;

1279 Synthesize Find similar

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Rx-ID: 5818064 Find similar reactions

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Shechter; Kaplan

Journal of the American Chemical Society, 1953 , vol. 75, p. 3980,3983 Full Text Show Details

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1280 Synthesize Find similar

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Rx-ID: 7441813 Find similar reactions

Criegee et al.

Justus Liebigs Annalen der Chemie, 1953 , vol. 583, p. 1,28 Full Text View citing articles Show Details

T=0°C;

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1281 Synthesize Find similar

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Rx-ID: 7441815 Find similar reactions

Criegee et al.

Justus Liebigs Annalen der Chemie, 1953 , vol. 583, p. 1,28 Full Text View citing articles Show Details

T=-30°C;

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1282 Synthesize Find similar Rx-ID: 7449254 Find similar reactions

Titow; Matweewa

Sb. Statei Obshch. Khim., 1953 , p. 246,248 Chem.Abstr., 1955 , p. 886 Full Text Show Details

1283 Synthesize Find similar

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Rx-ID: 8236271 Find similar reactions

West; Rochow

Naturwissenschaften, 1953 , vol. 40, p. 142 Full Text View citing articles Show Details

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1284 Synthesize Find similar

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Rx-ID: 60708 Find similar reactions

Cooper; Davison

Journal of the Chemical Society, 1952 , p. 1180 Full Text Show Details

T=30°C; untersucht wurde das Gleichgewicht;

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1285 Synthesize Find similar

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Rx-ID: 5818066 Find similar reactions

Bahner

Industrial and Engineering Chemistry, 1952 , vol. 44, p. 317 Full Text Show Details

Verwendung einer Platin-Anode.Electrolysis;

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1286 Synthesize Find similar Rx-ID: 7054812 Find similar reactions

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Cooper; Davison

Journal of the Chemical Society, 1952 , p. 1180 Full Text Show Details

1287 Synthesize Find similar

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Rx-ID: 8236268 Find similar reactions

Mousseron; Canet

Bulletin de la Societe Chimique de France, 1952 , p. 190,195 Full Text View citing articles Show Details