acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

Base Information

Chemical Name:acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester
CAS No.:733000-99-2
Molecular Formula:C₄₆H₆₀O₇Si
Molecular Weight:753.064
Hs Code.:

acetic acid 7-acetoxy-3-(<i>tert</i>-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1<i>H</i>-cyclopenta[<i>a</i>]phenanthren-6-yl ester

Synonyms:acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

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Chemical Property of acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

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Technology Process of acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

There total 3 articles about acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl 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: 57.0%

: 22037-28-1
3-bromofurane

: 733000-97-0
Acetic acid (3S,5S,6R,7R,8R,9S,10R,13S,14S)-7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-10,13-dimethyl-17-((S)-1-methyl-2-oxo-ethyl)-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

: 733000-99-2
acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

: 733000-98-1
acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

Guidance literature:: With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h;
DOI:10.1016/j.tet.2004.04.084

Reference yield:

: 537674-16-1
(Z)-6α,7β-(diacetoxy)-3β-[(tert-butyldiphenylsilyl)oxy]-5α-pregn-17(20)-ene

: 733000-99-2
acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / BF₃*Et₂O / CH₂Cl₂ / 0.5 h / -78 - -30 °C

2: 69 percent / PDC; 4 Angstroem molecular sieves / CH₂Cl₂ / 3 h / 20 °C

3: 28 percent / n-BuLi / hexane; tetrahydrofuran / 0.5 h / -78 °C

With dipyridinium dichromate; n-butyllithium; 4 A molecular sieve; boron trifluoride diethyl etherate; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1016/j.tet.2004.04.084

Reference yield:

: 537674-17-2
6α,7β-(diacetoxy)-3β-[(tert-butyldiphenylsilyl)oxy]-5α-23,24-bisnorchol-16-en-22-ol

: 733000-99-2
acetic acid 7-acetoxy-3-(tert-butyl-diphenyl-silanyloxy)-17-(2-furan-3-yl-2-hydroxy-1-methyl-ethyl)-10,13-dimethyl-2,3,4,5,6,7,8,9,10,11,12,13,14,15-tetradecahydro-1H-cyclopenta[a]phenanthren-6-yl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 69 percent / PDC; 4 Angstroem molecular sieves / CH₂Cl₂ / 3 h / 20 °C

2: 28 percent / n-BuLi / hexane; tetrahydrofuran / 0.5 h / -78 °C

With dipyridinium dichromate; n-butyllithium; 4 A molecular sieve; In tetrahydrofuran; hexane; dichloromethane;
DOI:10.1016/j.tet.2004.04.084