Reaxys
PubChem
eMolecules
Reactions (1470)
Yield
Substances (2)
Citations (3478)
Conditions
References A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1190 Synthesize Find similar
in cyclohexane; cyclohexene
Hide Experimental Procedure
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
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
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 ;
Hide Experimental Procedure
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
B
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 25265759 Find similar reactions
UBE Industries, Ltd.
Patent: US4010206 A1, 1977 ;
Hide Experimental Procedure
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
B
Synthesize Find similar
Synthesize Find similar
1194
Rx-ID: 25210725 Find similar reactions
BP Chemicals (U.K.) Limited
Patent: US3947406 A1, 1976 ;
Hide Experimental Procedure
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
B
Synthesize Find similar
Synthesize Find similar
1195
Rx-ID: 25212157 Find similar reactions
BP Chemicals International Limited
Patent: US3983142 A1, 1976 ;
Hide Experimental Procedure
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 25268090 Find similar reactions
BP Chemicals (U.K.) Limited
Patent: US3947406 A1, 1976 ;
in methanol
Hide Experimental Procedure
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
Synthesize Find similar
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
A
B
C
D
E
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
1198 Synthesize Find similar
Synthesize Find similar
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
A
B
C
D
E
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
1199 Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
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%
Synthesize Find similar
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
Synthesize Find similar
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
A
1203
B
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1204 Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1206 Synthesize Find similar Rx-ID: 714791
Synthesize Find similar
Synthesize Find similar
Find similar reactions
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
A
B
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Schultz
Journal of Organic Chemistry, 1960 , vol. 25, p. 1039,1040 Full Text Show Details
Behandeln des Reaktionsprodukts mit wss. Salzsaeure;
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
1211 Synthesize Find similar
Synthesize Find similar
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;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
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;
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
1215 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
1221 Synthesize Find similar
Synthesize Find similar
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
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
1222 Synthesize Find similar Rx-ID: 399717
Find similar reactions
Bennett et al.
Journal of the Chemical Society, 1958 , p. 4508,4513 Full Text Show Details
T=495°C; Pyrolysis;
A
B
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
1225 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5687525 Find similar reactions
Synthesize Find similar
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
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
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;
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 6680216 Find similar reactions
Kuhn; Haas
Justus Liebigs Annalen der Chemie, 1958 , vol. 611, p. 57,63 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1233 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 7054811 Find similar reactions
Kharasch; Sosnovsky
Journal of Organic Chemistry, 1958 , vol. 23, p. 1322,1324 Full Text Show Details
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
C
1235 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
Rx-ID: 8236278 Find similar reactions
B
1239
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Stuckwisch et al.
Journal of Organic Chemistry, 1957 , vol. 22, p. 1678 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
1242 Synthesize Find similar Rx-ID: 96646 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Urbanski et al.
Roczniki Chemii, 1957 , vol. 31, p. 93,96 Chem.Abstr., 1957 , p. 14717 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
1243 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
T=0°C; Rate constant;
Synthesize Find similar
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
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
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;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
1249 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
A
B
C
1250 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Hawthorne; Strahm
Journal of the American Chemical Society, 1957 , vol. 79, p. 2515,2517 Full Text Show Details
T=50°C; Rate constant;
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1253 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
1254 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 7054799 Find similar reactions
Pritzkow; Mueller
Chemische Berichte, 1956 , vol. 89, p. 2318,2319 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
1257 Synthesize Find similar
1258
Synthesize Find similar
Rx-ID: 7065967 Find similar reactions
Pritzkow; Mueller
Chemische Berichte, 1956 , vol. 89, p. 2318,2319 Full Text Show Details
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
1260 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1261 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1264 Synthesize Find similar
Synthesize Find similar
Rx-ID: 8236283 Find similar reactions
Taguchi; Kojima
Pharmaceutical Bulletin, 1955 , vol. 3, p. 351,353 Full Text Show Details
Solvolyse;
A
B
Synthesize Find similar
Synthesize Find similar
1265 Synthesize Find similar
Synthesize Find similar
Rx-ID: 8236284 Find similar reactions
Taguchi; Kojima
Pharmaceutical Bulletin, 1955 , vol. 3, p. 351,353 Full Text Show Details
Solvolyse;
A
B
Synthesize Find similar
Synthesize Find similar
1266 Synthesize Find similar
Solvolyse;
Synthesize Find similar
Rx-ID: 8236285 Find similar reactions
Taguchi; Kojima
Pharmaceutical Bulletin, 1955 , vol. 3, p. 351,353
Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
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
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
1272 Synthesize Find similar
Synthesize Find similar
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
A
B
Synthesize Find similar
Synthesize Find similar
1273 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Behandeln des Reaktionsprodukts mit Natriumhydrogensulfit, Magnesiumhydroxid und Wasser;
A
Synthesize Find similar
B
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
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Grob; Schmid
Helvetica Chimica Acta, 1953 , vol. 36, p. 1763,1769 Full Text Show Details
1278 Synthesize Find similar
Synthesize Find similar
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;
A
B
1279 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Rx-ID: 5818064 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Shechter; Kaplan
Journal of the American Chemical Society, 1953 , vol. 75, p. 3980,3983 Full Text Show Details
A
B
Synthesize Find similar
Synthesize Find similar
1280 Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1281 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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;
A
B
C
D
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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
Synthesize Find similar
Synthesize Find similar
Rx-ID: 8236271 Find similar reactions
West; Rochow
Naturwissenschaften, 1953 , vol. 40, p. 142 Full Text View citing articles Show Details
A
B
Synthesize Find similar
Synthesize Find similar
1284 Synthesize Find similar
Synthesize Find similar
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;
A
B
C
Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
1285 Synthesize Find similar
Synthesize Find similar
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;
A
B
Synthesize Find similar
Synthesize Find similar
1286 Synthesize Find similar Rx-ID: 7054812 Find similar reactions
Synthesize Find similar
Synthesize Find similar
Cooper; Davison
Journal of the Chemical Society, 1952 , p. 1180 Full Text Show Details
1287 Synthesize Find similar
Synthesize Find similar
Synthesize Find similar
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