(2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol

Base Information

Chemical Name:(2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol
CAS No.:210286-10-5
Molecular Formula:C₃₁H₄₀O₆Si
Molecular Weight:536.74
Hs Code.:

Synonyms:(2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol

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Chemical Property of (2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol

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Technology Process of (2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol

There total 1 articles about (2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-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: 91.0%

: 58479-61-1
tert-butylchlorodiphenylsilane

: 210286-09-2
(2R,3S,4S,5S)-3-benzyloxy-4-hydroxy-5-hydroxymethyl-2-dimethoxymethyl-tetrahydrofuran

: 210286-10-5
(2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; for 3h; Ambient temperature;
DOI:10.1016/S0040-4020(98)00336-6

Reference yield: 67.0%

: 100-39-0
benzyl bromide

: 210286-10-5
(2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol

: 210286-11-6
((2S,3R,4S,5R)-3,4-Bis-benzyloxy-5-dimethoxymethyl-tetrahydro-furan-2-ylmethoxy)-tert-butyl-diphenyl-silane

Guidance literature:: With silver(l) oxide; In N,N-dimethyl-formamide; for 3h; Ambient temperature;
DOI:10.1016/S0040-4020(98)00336-6

Reference yield:

: 210286-10-5
(2S,3R,4S,5R)-4-Benzyloxy-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-dimethoxymethyl-tetrahydro-furan-3-ol

: 210286-12-7
((2S,3R,4S,5R)-3,4-Bis-benzyloxy-5-dimethoxymethyl-tetrahydro-furan-2-yl)-methanol

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / Ag₂O / dimethylformamide / 3 h / Ambient temperature

2: 94 percent / TBAF / tetrahydrofuran / 18 h / Ambient temperature

With tetrabutyl ammonium fluoride; silver(l) oxide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(98)00336-6