(2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate

Base Information

Chemical Name:(2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate
CAS No.:75671-00-0
Molecular Formula:C₂₈H₄₂O₈SSi
Molecular Weight:566.788
Hs Code.:

Synonyms:(2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate

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Chemical Property of (2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate

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Technology Process of (2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate

There total 7 articles about (2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate 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: 80.0%

: 124-63-0
methanesulfonyl chloride

: 111727-15-2
(2R,3R,4S,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-ol

: 75671-00-0
(2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1039/c4ra04845h

Reference yield:

: 18162-48-6
tert-butyldimethylsilyl chloride

: 75671-00-0
(2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: 1H-imidazole / dichloromethane / 0.5 h / 0 °C

2: triethylamine / dichloromethane / 1 h / 0 °C

With 1H-imidazole; triethylamine; In dichloromethane;
DOI:10.1039/c4ra04845h

Reference yield:

: 97-30-3
methyl-alpha-D-glucopyranoside

: 75671-00-0
(2R,3R,4R,5R,6S)-4,5-bis(benzyloxy)-2-((tert-butyldimethylsilyloxy)methyl)-6-methoxytetrahydro-2H-pyran-3-yl methanesulfonate

Guidance literature:: Multi-step reaction with 5 steps

1: camphor-10-sulfonic acid / acetone

2: sodium hydride / N,N-dimethyl-formamide

3: iodine / methanol / Reflux

4: 1H-imidazole / dichloromethane / 0.5 h / 0 °C

5: triethylamine / dichloromethane / 1 h / 0 °C

With 1H-imidazole; camphor-10-sulfonic acid; iodine; sodium hydride; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1039/c4ra04845h