(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

Base Information

Chemical Name:(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate
CAS No.:1454816-25-1
Molecular Formula:C₂₁H₃₀O₄
Molecular Weight:346.467
Hs Code.:

Synonyms:(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

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Chemical Property of (S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

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Technology Process of (S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

There total 3 articles about (S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate 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:

: 1454816-52-4
(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

: 1454816-25-1
(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

Guidance literature:: With camphor-10-sulfonic acid; In methanol;
DOI:10.1016/j.bmcl.2013.07.054

Reference yield:

: 189102-76-9
de-A,B-8β,22-di-[(tert-butyldimethyl)silyloxy]-23,24-dinorcholane

: 1454816-25-1
(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

Guidance literature:: Multi-step reaction with 3 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran

2: dicyclohexyl-carbodiimide; dmap / dichloromethane / 20 °C

3: camphor-10-sulfonic acid / methanol

With dmap; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.bmcl.2013.07.054

Reference yield:

: 64190-52-9
(8S,20S)-de-A,B-20-(hydroxymethyl)pregnan-8-ol

: 1454816-25-1
(S)-2-((1R,3aR,4S,7aR)-4-((tert-butyldimethylsilyl)oxy)-7a-methyloctahydro-1H-inden-1-yl)propyl 3-methoxybenzoate

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane

2: tetrabutyl ammonium fluoride / tetrahydrofuran

3: dicyclohexyl-carbodiimide; dmap / dichloromethane / 20 °C

4: camphor-10-sulfonic acid / methanol

With dmap; camphor-10-sulfonic acid; tetrabutyl ammonium fluoride; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/j.bmcl.2013.07.054