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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 440712Generated: October 26, 2026

Methanesulfonyl chloride → 3,5-di-O-benzyl-2-deoxy-4-O-methane-sulphonyl-L-threo-pentose dibenzyl dithioacetal

https://huagongshe.com/reaction/440712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetalHCID 15059957—
SolventPyridineHCID 1049—
Product3,5-di-O-benzyl-2-deoxy-4-O-methane-sulphonyl-L-threo-pentose dibenzyl dithioacetalHCID 15059960—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3,5-di-O-benzyl-2-deoxy-L-threo-pentose dibenzyl dithioacetal (61.4 g, 113 mmol) in dry pyridine (700 ml) was added methanesulphonyl chloride (19.4 g, 169 mmol) in dry pyridine (200 ml) dropwise, with stirring, at 0° C. The temperature of the mixture was raised to room temperature and stirring continued for 18 hours. The pyridine was then removed in vacuo and the residue dissolved in dichloromethane. The dichloromethane extracts were then successively washed with 2M hydrochloric acid, 1M sodium carbonate and water, dried (magnesium sulphate) and evaporated to give the title product as a thick viscous syrup. A sample of this was crystallised from hexane-ethyl acetate to give the title product as white crystals, m.p 82°-83° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521163
Source datasetuspto-grants-1996_05
ORD IDord-c9b256705bed443288b6f29296ee4bdd
Source noteuspto-grants-1996_05