(E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol

Base Information

Chemical Name:(E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol
CAS No.:384817-51-0
Molecular Formula:C₃₂H₄₆O₂Si
Molecular Weight:490.802
Hs Code.:

Synonyms:(E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol

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Chemical Property of (E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol

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Technology Process of (E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol

There total 5 articles about (E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-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: 99.0%

: 384817-50-9
(E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-enoic acid ethyl ester

: 384817-51-0
(E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; at 20 ℃; for 0.5h;
DOI:10.1016/S0040-4039(01)01608-2

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 384817-51-0
(E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / imidazole / CH₂Cl₂ / 2 h / 20 °C

2: 99 percent / LiAlH₄ / diethyl ether / 0.5 h / 20 °C

With 1H-imidazole; lithium aluminium tetrahydride; In diethyl ether; dichloromethane;
DOI:10.1016/S0040-4039(01)01608-2

Reference yield:

: 380414-34-6
(E)-4-[(1R,5R,6R)-6-dimethoxymethyl-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-enoic acid

: 384817-51-0
(E)-4-[(1R,5R,6R)-6-(tert-Butyl-diphenyl-silanyloxymethyl)-5-isopropyl-2-methyl-cyclohex-2-enyl]-2-methyl-but-2-en-1-ol

Guidance literature:: Multi-step reaction with 4 steps

1: 99 percent / aq. AcOH / tetrahydrofuran / 17 h / 20 °C

2: 93 percent / NaBH₄ / ethanol / 0.25 h / 20 °C

3: 86 percent / imidazole / CH₂Cl₂ / 2 h / 20 °C

4: 99 percent / LiAlH₄ / diethyl ether / 0.5 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; lithium aluminium tetrahydride; acetic acid; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane;
DOI:10.1016/S0040-4039(01)01608-2