(1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

Base Information

Chemical Name:(1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester
CAS No.:141397-07-1
Molecular Formula:C₃₄H₃₈O₆
Molecular Weight:542.672
Hs Code.:

(1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

Synonyms:(1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

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Chemical Property of (1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

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Technology Process of (1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

There total 4 articles about (1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester 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:

Reference yield: 87.0%

: 141411-05-4,141505-43-3
C₃₄H₄₀O₅

: 141397-07-1
(1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

Guidance literature:: With chromium(VI) oxide; acetic acid; In dichloromethane; at -20 ℃; for 1h;
DOI:10.1021/jo00040a050

Reference yield:

: 71388-83-5
p-benzoyl-2,3-dihydrocinnamic acid

: 141397-07-1
(1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / DMAP, DCC / diethyl ether; CH₂Cl₂ / 8 h

2: 95 percent / benzene / 1 h / Irradiation

3: 87 percent / CrO₃, CH₃COOH / CH₂Cl₂ / 1 h / -20 °C

With chromium(VI) oxide; dmap; acetic acid; dicyclohexyl-carbodiimide; In diethyl ether; dichloromethane; benzene;
DOI:10.1021/jo00040a050

Reference yield:

: 141396-79-4
(1R,2S,4aR,8aR,10aR)-2-Hydroxy-1,4a-dimethyl-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

: 141397-07-1
(1R,2S,4aR,8aS,10aR)-2-[3-(4-Benzoyl-phenyl)-propionyloxy]-1,4a-dimethyl-6-oxo-1,3,4,4a,6,7,8,9,10,10a-decahydro-2H-phenanthrene-8a-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 86 percent / DMAP, DCC / diethyl ether; CH₂Cl₂ / 8 h

2: 95 percent / benzene / 1 h / Irradiation

3: 87 percent / CrO₃, CH₃COOH / CH₂Cl₂ / 1 h / -20 °C

With chromium(VI) oxide; dmap; acetic acid; dicyclohexyl-carbodiimide; In diethyl ether; dichloromethane; benzene;
DOI:10.1021/jo00040a050