(4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

Base Information

Chemical Name:(4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol
CAS No.:185909-46-0
Molecular Formula:C₂₁H₃₆O₄Si
Molecular Weight:380.6
Hs Code.:

Synonyms:(4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

There total 5 articles about (4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-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: 79.0%

: 24850-33-7
allyltributylstanane

: 185909-45-9
(S)-4-(tert-Butyl-dimethyl-silanyloxy)-3-(4-methoxy-benzyloxy)-butyraldehyde

: (4R,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

: 185909-46-0
(4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

Guidance literature:: With titanium(IV) isopropylate; (S)-[1,1']-binaphthalenyl-2,2'-diol; In dichloromethane; at -20 ℃; for 144h;
DOI:10.1016/S0040-4039(96)02110-7

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 185909-46-0
(4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

Guidance literature:: Multi-step reaction with 5 steps

1: imidazole / dimethylformamide

2: CSA / CH₂Cl₂

3: LiAlH₄ / tetrahydrofuran / 0 °C

4: (COCl)2, DMSO, Et₃N / CH₂Cl₂ / -78 °C

5: 79 percent / Ti(OiPr)4, (S)-BINOL / CH₂Cl₂ / 144 h / -20 °C

With 1H-imidazole; titanium(IV) isopropylate; lithium aluminium tetrahydride; oxalyl dichloride; camphor-10-sulfonic acid; (S)-[1,1']-binaphthalenyl-2,2'-diol; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4039(96)02110-7

Reference yield:

: 113494-89-6
methyl (S)-4-<(1,1-dimethylethyl)dimethylsiloxy>-3-hydroxybutanoate

: 185909-46-0
(4S,6S)-7-(tert-Butyl-dimethyl-silanyloxy)-6-(4-methoxy-benzyloxy)-hept-1-en-4-ol

Guidance literature:: Multi-step reaction with 4 steps

1: CSA / CH₂Cl₂

2: LiAlH₄ / tetrahydrofuran / 0 °C

3: (COCl)2, DMSO, Et₃N / CH₂Cl₂ / -78 °C

4: 79 percent / Ti(OiPr)4, (S)-BINOL / CH₂Cl₂ / 144 h / -20 °C

With titanium(IV) isopropylate; lithium aluminium tetrahydride; oxalyl dichloride; camphor-10-sulfonic acid; (S)-[1,1']-binaphthalenyl-2,2'-diol; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4039(96)02110-7