Technology Process of 12-Tridecenoic acid, 3,7-dihydroxy-4,4,6,8,12-pentamethyl-5-oxo-,
(1S,5S)-5-ethenyl-2-methyl-3-phenyl-2-cyclopenten-1-yl ester,
(3S,6R,7S,8S)-
There total 18 articles about 12-Tridecenoic acid, 3,7-dihydroxy-4,4,6,8,12-pentamethyl-5-oxo-,
(1S,5S)-5-ethenyl-2-methyl-3-phenyl-2-cyclopenten-1-yl ester,
(3S,6R,7S,8S)- which
guide to synthetic route it.
The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
synthetic route:
-
-
923956-13-2
(3S,6R,7S,8S)-3,7-dihydroxy-4,4,6,8,12-pentamethyl-5-oxotridec-12-enoic acid (1S,2E,5S)-2-methyl-3-phenyl-5-vinylcyclopent-2-enyl ester
- Guidance literature:
-
C38H60O5Si;
With
tris(dimethylamino)sulfonium trimethylsilyldifluoride;
In
ethanol; ethyl acetate; N,N-dimethyl-formamide;
for 24h;
With
water;
In
ethanol; ethyl acetate; N,N-dimethyl-formamide;
pH=7;
-
-
923956-13-2
(3S,6R,7S,8S)-3,7-dihydroxy-4,4,6,8,12-pentamethyl-5-oxotridec-12-enoic acid (1S,2E,5S)-2-methyl-3-phenyl-5-vinylcyclopent-2-enyl ester
- Guidance literature:
-
Multi-step reaction with 4 steps
1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C
2: dmap; dicyclohexyl-carbodiimide / dichloromethane / 16.25 h / 0 - 20 °C
3: ammonium chloride; zinc / ethanol / 0.75 h / 20 °C
4: tris(dimethylamino)sulfonium trimethylsilyldifluoride / N,N-dimethyl-formamide / 48 h
With
dmap; tetrabutyl ammonium fluoride; tris(dimethylamino)sulfonium trimethylsilyldifluoride; ammonium chloride; dicyclohexyl-carbodiimide; zinc;
In
tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
-
-
923956-13-2
(3S,6R,7S,8S)-3,7-dihydroxy-4,4,6,8,12-pentamethyl-5-oxotridec-12-enoic acid (1S,2E,5S)-2-methyl-3-phenyl-5-vinylcyclopent-2-enyl ester
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: diisobutylaluminium hydride / hexane; toluene / 1 h / -78 °C
2.1: n-butyllithium / tetrahydrofuran; hexanes / 0.5 h / 0 °C
2.2: 0.5 h / 0 °C
3.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 0.5 h / 0 °C
4.1: dmap; dicyclohexyl-carbodiimide / dichloromethane / 16.25 h / 0 - 20 °C
5.1: ammonium chloride; zinc / ethanol / 0.75 h / 20 °C
6.1: tris(dimethylamino)sulfonium trimethylsilyldifluoride / N,N-dimethyl-formamide / 48 h
With
dmap; n-butyllithium; tetrabutyl ammonium fluoride; tris(dimethylamino)sulfonium trimethylsilyldifluoride; diisobutylaluminium hydride; ammonium chloride; dicyclohexyl-carbodiimide; zinc;
In
tetrahydrofuran; hexanes; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide; toluene;