(1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene

Base Information

Chemical Name:(1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene
CAS No.:169191-16-6
Molecular Formula:C₂₅H₄₀O₄S₂Si
Molecular Weight:496.808
Hs Code.:

Synonyms:(1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene

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Chemical Property of (1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene

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Technology Process of (1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene

There total 4 articles about (1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene 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:

: 89291-76-9
(1S,4R,5S)-(-)-3-<(benzyloxy)methyl>-4,5-O-isopropylidene-2-cyclopenten-1-ol

: 169191-16-6
(1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene

Guidance literature:: Multi-step reaction with 3 steps

1: 54 percent / CH₂Cl₂; toluene / -78 deg C, rt, 18 h

2: 87.4 percent / imidazole / dimethylformamide / 0.67 h / Ambient temperature

3: 2.) NaH / 1.) THF, 0 deg C, 5 min, 2.) rt, 60 min

With 1H-imidazole; sodium hydride; In dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1080/07328319608002382

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 169191-16-6
(1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene

Guidance literature:: Multi-step reaction with 2 steps

1: 87.4 percent / imidazole / dimethylformamide / 0.67 h / Ambient temperature

2: 2.) NaH / 1.) THF, 0 deg C, 5 min, 2.) rt, 60 min

With 1H-imidazole; sodium hydride; In N,N-dimethyl-formamide;
DOI:10.1080/07328319608002382

Reference yield:

: 169191-14-4
(1S,4R,5S)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-hydroxy-2-cyclopenten-1-ol

: 169191-16-6
(1S,4R,5S)-1-(tert-butyldimethylsilyloxy)-3-<(benzyloxy)methyl>-4-tert-butyloxy-5-<(methylthio)thiocarbonyloxy>-2-cyclopentene

Guidance literature:: Multi-step reaction with 2 steps

1: 87.4 percent / imidazole / dimethylformamide / 0.67 h / Ambient temperature

2: 2.) NaH / 1.) THF, 0 deg C, 5 min, 2.) rt, 60 min

With 1H-imidazole; sodium hydride; In N,N-dimethyl-formamide;
DOI:10.1080/07328319608002382