5,7,17-Trioxa-2-silaoctadec-10-en-13-ol, 8-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-18-(4-methoxyphenyl)-2, 2,11,15-tetramethyl-, (8S,10Z,15S)-

Base Information

Chemical Name:5,7,17-Trioxa-2-silaoctadec-10-en-13-ol, 8-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-18-(4-methoxyphenyl)-2, 2,11,15-tetramethyl-, (8S,10Z,15S)-
CAS No.:396092-34-5
Molecular Formula:C32H60O6Si2
Molecular Weight:596.996
Hs Code.:

5,7,17-Trioxa-2-silaoctadec-10-en-13-ol,
8-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-18-(4-methoxyphenyl)-2,
2,11,15-tetramethyl-, (8S,10Z,15S)-

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Chemical Property of 5,7,17-Trioxa-2-silaoctadec-10-en-13-ol, 8-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-18-(4-methoxyphenyl)-2, 2,11,15-tetramethyl-, (8S,10Z,15S)-

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Technology Process of 5,7,17-Trioxa-2-silaoctadec-10-en-13-ol, 8-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-18-(4-methoxyphenyl)-2, 2,11,15-tetramethyl-, (8S,10Z,15S)-

There total 12 articles about 5,7,17-Trioxa-2-silaoctadec-10-en-13-ol, 8-[[[(1,1-dimethylethyl)dimethylsilyl]oxy]methyl]-18-(4-methoxyphenyl)-2, 2,11,15-tetramethyl-, (8S,10Z,15S)- 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: 53.0%

: 396092-33-4
(5S)-6-tert-butyldimethylsilyloxy-5-(2-trimethylsilylethoxy)-methoxy-2-methylhex-2-enyl(tributyl)stannane

: (3S)-4-((4-methoxybenzyl)oxy)-3-methylbutanal

: 396092-34-5
(2S,9S,6Z)-10-tert-butyldimethylsilyloxy-1-(4-methoxybenzyl)oxy-2,6-dimethyl-9-(2-trimethylsilylethoxy)methoxydec-6-en-4-ol

Guidance literature:: (5S)-6-tert-butyldimethylsilyloxy-5-(2-trimethylsilylethoxy)-methoxy-2-methylhex-2-enyl(tributyl)stannane; With stannic bromide; In dichloromethane; at -78 ℃; for 0.0833333h;

(3S)-4-((4-methoxybenzyl)oxy)-3-methylbutanal; In dichloromethane; at -78 ℃; for 0.5h;
DOI:10.1039/c2ob26310f

Reference yield:

: 396092-18-5
(2S)-5-methyl-4-(phenylsulfonyl)hex-5-ene-1,2-diol

: 396092-34-5
(2S,9S,6Z)-10-tert-butyldimethylsilyloxy-1-(4-methoxybenzyl)oxy-2,6-dimethyl-9-(2-trimethylsilylethoxy)methoxydec-6-en-4-ol

Guidance literature:: Multi-step reaction with 3 steps

1.1: imid.

2.1: 78 percent / i-Pr₂EtN

3.1: Bu₃SnH; AIBN

3.2: SnBr₄ / -78 °C

With 1H-imidazole; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; N-ethyl-N,N-diisopropylamine;
DOI:10.1016/S0040-4039(01)01795-6

Reference yield:

: 396092-19-6
(2S)-1-tert-butyldimethylsilyloxy-5-methyl-4-(phenylsulfonyl)hex-5-en-2-ol

: 396092-34-5
(2S,9S,6Z)-10-tert-butyldimethylsilyloxy-1-(4-methoxybenzyl)oxy-2,6-dimethyl-9-(2-trimethylsilylethoxy)methoxydec-6-en-4-ol

Guidance literature:: Multi-step reaction with 2 steps

1.1: 78 percent / i-Pr₂EtN

2.1: Bu₃SnH; AIBN

2.2: SnBr₄ / -78 °C

With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; N-ethyl-N,N-diisopropylamine;
DOI:10.1016/S0040-4039(01)01795-6