(2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

Base Information

Chemical Name:(2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol
CAS No.:149933-67-5
Molecular Formula:C₃₉H₅₃NO₃Si
Molecular Weight:611.94
Hs Code.:

(2S,3S,4E)-2-<N-(diphenylmethylene)amino>-3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

Synonyms:(2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

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Chemical Property of (2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

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Technology Process of (2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

There total 1 articles about (2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol 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: 75.0%

: 98-88-4
benzoyl chloride

: 143428-50-6
(2S,3S,4E)-2--1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

: 149933-67-5
(2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

Guidance literature:: With pyridine; dmap; Ambient temperature;
DOI:10.1021/jo00068a028

Reference yield: 62.0%

: 149933-67-5
(2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

: 149933-69-7
(2S,3S,4E)-2--1-O-benzoyl-4-tridecene-1,3-diol

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; Ambient temperature;
DOI:10.1021/jo00068a028

Reference yield:

: 149933-67-5
(2S,3S,4E)-2--3-O-benzoyl-1-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

: (2S,3S,4E)-2--1-O-benzoyl-3-O-(tert-butyldimethylsilyl)-4-tridecene-1,3-diol

Guidance literature:: Multi-step reaction with 2 steps

1: 62 percent / TBAF / tetrahydrofuran / Ambient temperature

2: 97 percent / imidazole / dimethylformamide / 48 h / Ambient temperature

With 1H-imidazole; tetrabutyl ammonium fluoride; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1021/jo00068a028