(1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol

Base Information

Chemical Name:(1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol
CAS No.:423764-39-0
Molecular Formula:C₁₈H₃₂O₂Si
Molecular Weight:308.536
Hs Code.:

Synonyms:(1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol

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Chemical Property of (1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol

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Technology Process of (1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol

There total 1 articles about (1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol 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: 70.0%

: 1112-56-7
tetravinyltin (IV)

: 423764-38-9
(5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-cyclohex-2-enone

: 423764-39-0
(1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol

Guidance literature:: tetravinyltin (IV); With n-butyllithium; In tetrahydrofuran; at 20 ℃; for 1h;

(5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-cyclohex-2-enone; In tetrahydrofuran; at 20 ℃; for 6h; Further stages.;
DOI:10.1021/jo010752r

Reference yield: 90.0%

: 423764-39-0
(1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol

: 423764-68-5
(1R,2S,6R)-6-Isopropenyl-3-methyl-2-vinyl-cyclohex-3-ene-1,2-diol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 0.5h;
DOI:10.1021/jo010752r

Reference yield:

: 423764-39-0
(1S,5R,6R)-6-(tert-Butyl-dimethyl-silanyloxy)-5-isopropenyl-2-methyl-1-vinyl-cyclohex-2-enol

: 423764-69-6
(1S,5R,6R)-5-Isopropenyl-6-(2-methoxy-ethoxymethoxy)-2-methyl-1-vinyl-cyclohex-2-enol

Guidance literature:: Multi-step reaction with 2 steps

1: 90 percent / TBAF / tetrahydrofuran / 0.5 h / 20 °C

2: 60 percent / ethyldiisopropylamine / CH₂Cl₂ / 16 h / 20 °C

With tetrabutyl ammonium fluoride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo010752r