Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

Base Information

Chemical Name:Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester
CAS No.:117168-32-8
Molecular Formula:C₄₁H₆₁F₃O₆SSi
Molecular Weight:767.078
Hs Code.:

Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

Synonyms:Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

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Chemical Property of Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

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Technology Process of Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

There total 7 articles about Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-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: 98.0%

: 358-23-6
trifluoromethylsulfonic anhydride

: Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-oxo-2,3,4,5,6,7,9,10,11,12,13,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

: 117168-32-8
Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

Guidance literature:: With 2,6-di-tert-butyl-4-methylpyridine; In dichloromethane; Heating;
DOI:10.1039/c39880000019

Reference yield:

: 563-80-4
3-methyl-butan-2-one

: 117168-32-8
Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

Guidance literature:: Multi-step reaction with 6 steps

1: LDA / tetrahydrofuran / -78 °C

2: p-MeC₆H₄SO₃H / toluene; CHCl₃ / 60 - 70 °C

3: H₂ / Lindlar catalyst

4: tBuNH₂*BH₃ / CH₂Cl₂ / Heating

5: 2,6-lutidine / CH₂Cl₂ / 0 °C

6: 98 percent / 2,6-di-t-butyl-4-methylpyridine / CH₂Cl₂ / Heating

With 2,6-dimethylpyridine; 2,6-di-tert-butyl-4-methylpyridine; N-tert-butylaminoborane; hydrogen; toluene-4-sulfonic acid; lithium diisopropyl amide; Lindlar's catalyst; In tetrahydrofuran; dichloromethane; chloroform; toluene;
DOI:10.1039/c39880000019

Reference yield:

: Benzoic acid (3S,5S,10S,13R,17R)-10,13-dimethyl-17-((S)-1-methyl-2-oxo-ethyl)-15-oxo-2,3,4,5,6,7,9,10,11,12,13,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

: 117168-32-8
Benzoic acid (3S,5S,10S,13R,17R)-17-[(R)-4-(tert-butyl-dimethyl-silanyloxy)-1,5-dimethyl-hexyl]-10,13-dimethyl-15-trifluoromethanesulfonyloxy-2,3,4,5,6,7,10,11,12,13,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl ester

Guidance literature:: Multi-step reaction with 6 steps

1: LDA / tetrahydrofuran / -78 °C

2: p-MeC₆H₄SO₃H / toluene; CHCl₃ / 60 - 70 °C

3: H₂ / Lindlar catalyst

4: tBuNH₂*BH₃ / CH₂Cl₂ / Heating

5: 2,6-lutidine / CH₂Cl₂ / 0 °C

6: 98 percent / 2,6-di-t-butyl-4-methylpyridine / CH₂Cl₂ / Heating

With 2,6-dimethylpyridine; 2,6-di-tert-butyl-4-methylpyridine; N-tert-butylaminoborane; hydrogen; toluene-4-sulfonic acid; lithium diisopropyl amide; Lindlar's catalyst; In tetrahydrofuran; dichloromethane; chloroform; toluene;
DOI:10.1039/c39880000019