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

Base Information

Chemical Name:(E)-(4S,5R,6S)-6-(tert-butyldiphenylsilanoxy)-5-methylnon-1,7-diene-4-ol
CAS No.:343262-83-9
Molecular Formula:C₂₆H₃₆O₂Si
Molecular Weight:408.656
Hs Code.:

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

Chemical Property:

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Technology Process of (E)-(4S,5R,6S)-6-(tert-butyldiphenylsilanoxy)-5-methylnon-1,7-diene-4-ol

There total 4 articles about (E)-(4S,5R,6S)-6-(tert-butyldiphenylsilanoxy)-5-methylnon-1,7-diene-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: 85.0%

: 106356-53-0
B-allyldiisopinocampheylborane

: 343262-57-7
(E)-(2S,3R)-3-(tert-butyldiphenylsilanoxy)-2-methylhex-4-enal

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

Guidance literature:: In diethyl ether; at -78 ℃; for 3h;
DOI:10.1021/ol015753k

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

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

Guidance literature:: Multi-step reaction with 4 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

With 1H-imidazole; lithium borohydride; oxalyl dichloride; 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

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

Guidance literature:: Multi-step reaction with 4 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

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