(1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol

Base Information

Chemical Name:(1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol
CAS No.:874350-02-4
Molecular Formula:C₃₁H₅₆O₄Si₂
Molecular Weight:548.954
Hs Code.:

Synonyms:(1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol

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Chemical Property of (1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol

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Technology Process of (1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol

There total 3 articles about (1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol 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: 86.0%

: 874349-99-2
(1R,3S,5S)-1-[2-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-methylene-5-triisopropylsilanyloxy-cyclohexane-1,3-diol

: 100-39-0
benzyl bromide

: 874350-02-4
(1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1002/chem.200500640

Reference yield:

: 773889-91-1
(6R,7S,8S,10S)-7,8-epoxy-2,2,7-trimethyl-10-tri-isopropylsilyloxy-1,3-dioxaspiro[5.5]undecane

: 874350-02-4
(1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 61 percent / 2,2,6,6-tetramethylpiperidine; n-BuLi; Et₂AlCl / hexane; benzene; toluene / 0.75 h / 0 °C

2: 93 percent / imidazole / toluene; dimethylformamide / 15 h / 20 °C

3: 86 percent / NaH / dimethylformamide / 0 - 20 °C

With 2,2,6,6-tetramethyl-piperidine; 1H-imidazole; n-butyllithium; diethylaluminium chloride; sodium hydride; In hexane; N,N-dimethyl-formamide; toluene; benzene;
DOI:10.1002/chem.200500640

Reference yield:

: 773889-88-6
(1R,3S,5S)-1-(2-hydroxyethyl)-5-tri-isopropylsilyloxy-2-methylenecyclohexan-1,3-diol

: 874350-02-4
(1R,3S,5S)-1-(2-tert-butyldimethylsilyloxyethyl)-3-benzyloxy-5-triisopropylsilyloxy-2-methylencyclohexan-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 93 percent / imidazole / toluene; dimethylformamide / 15 h / 20 °C

2: 86 percent / NaH / dimethylformamide / 0 - 20 °C

With 1H-imidazole; sodium hydride; In N,N-dimethyl-formamide; toluene;
DOI:10.1002/chem.200500640