tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane

Base Information

Chemical Name:tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane
CAS No.:343262-58-8
Molecular Formula:C₃₄H₄₄O₃Si
Molecular Weight:528.807
Hs Code.:

Synonyms:tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane

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Chemical Property of tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane

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Technology Process of tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane

There total 5 articles about tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane 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: 67.0%

: 89238-99-3
O-(4-methoxybenzyl)-trichloroacetimidate

: 343262-83-9
(E)-(4S,5R,6S)-6-(tert-butyldiphenylsilanoxy)-5-methylnon-1,7-diene-4-ol

: 343262-58-8
tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane

Guidance literature:: With camphor-10-sulfonic acid; In dichloromethane; for 40h;
DOI:10.1021/ol015753k

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 343262-58-8
tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / imidazole / CH₂Cl₂ / 20 h

2: 86 percent / LiBH₄ / diethyl ether; H₂O / -20 - 5 °C

3: 98 percent / dimethylsulfoxide; oxalyl chloride; triethylamine / CH₂Cl₂ / -78 - -30 °C

4: 85 percent / diethyl ether / 3 h / -78 °C

5: 67 percent / CSA / CH₂Cl₂ / 40 h

With 1H-imidazole; lithium borohydride; oxalyl dichloride; camphor-10-sulfonic acid; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane; water; 3: Swern oxidation;
DOI:10.1021/ol015753k

Reference yield:

: 251318-99-7
(S)-4-Benzyl-3-((E)-(2S,3R)-3-hydroxy-2-methyl-hex-4-enoyl)-oxazolidin-2-one

: 343262-58-8
tert-Butyl-[(1R,2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-1-((E)-propenyl)-hex-5-enyloxy]-diphenyl-silane

Guidance literature:: Multi-step reaction with 5 steps

1: 99 percent / imidazole / CH₂Cl₂ / 20 h

2: 86 percent / LiBH₄ / diethyl ether; H₂O / -20 - 5 °C

3: 98 percent / dimethylsulfoxide; oxalyl chloride; triethylamine / CH₂Cl₂ / -78 - -30 °C

4: 85 percent / diethyl ether / 3 h / -78 °C

5: 67 percent / CSA / CH₂Cl₂ / 40 h

With 1H-imidazole; lithium borohydride; oxalyl dichloride; camphor-10-sulfonic acid; dimethyl sulfoxide; triethylamine; In diethyl ether; dichloromethane; water; 3: Swern oxidation;
DOI:10.1021/ol015753k