(2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol

Base Information

Chemical Name:(2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol
CAS No.:165683-84-1
Molecular Formula:C₂₁H₄₃NO₄Si
Molecular Weight:401.662
Hs Code.:

Synonyms:(2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol

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Chemical Property of (2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol

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Technology Process of (2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol

There total 8 articles about (2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol 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: 83.0%

: 18162-48-6
tert-butyldimethylsilyl chloride

: 104882-03-3
(2S,3S)-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-1,2-butanediol

: 165683-84-1
(2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃; for 48h;
DOI:10.1021/jo960351p

Reference yield:

: 178421-69-7
(2S,3S)-3-azido-4-cyclohexyl-1,2-butanediol

: 165683-84-1
(2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol

Guidance literature:: Multi-step reaction with 2 steps

1: 97 percent / H₂ / Pd/C / ethyl acetate / 18 h / 760 Torr

2: 83 percent / imidazole / dimethylformamide / 48 h / 20 °C

With 1H-imidazole; hydrogen; palladium on activated charcoal; In ethyl acetate; N,N-dimethyl-formamide; 1: Hydrogenolysis / 2: silylation;
DOI:10.1021/jo960351p

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 165683-84-1
(2S,3S)-1-[(tert-butyldimethylsilyl)oxy]-3-[(tert-butoxycarbonyl)amino]-4-cyclohexyl-2-butanol

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / H₂ / Pd(OH)2/C / ethyl acetate / 760 Torr

2: 83 percent / imidazole / dimethylformamide / 48 h / 20 °C

With 1H-imidazole; hydrogen; palladium dihydroxide; In ethyl acetate; N,N-dimethyl-formamide; 1: Hydrogenolysis / 2: silylation;
DOI:10.1021/jo960351p