Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1600147Generated: October 31, 2026

Sodium borohydride → 1,4-Anhydro-2-S-[(4-methoxyphenyl)methyl]-2-thio-L-arabinitol

https://huagongshe.com/reaction/1600147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2,5-Anhydro-4-S-[(4-methoxyphenyl)methyl]-4-thio-L-lyxoseHCID 88337316—
SolventEthanolHCID 702—
Product1,4-Anhydro-2-S-[(4-methoxyphenyl)methyl]-2-thio-L-arabinitolHCID 6764833569.9%

Reaction Steps

To a room temperature solution, under argon, of 10.9 g of product from Example 322 in 115 ml of absolute ethyl alcohol is added 1.57 g of sodium borohydride. The reaction is stirred at room temperature for 1 hour. Wateris added dropwise with stirring and the mixture is concentrated in vacuo. The residue is extracted with methylene chloride, washed with water, driedand concentrated in vacuo to give after chromatography (Silica gel: 50-75% ethyl acetate/hexane) 7.68 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05744465
Source datasetuspto-grants-1998_04
ORD IDord-47e9fcdbb80d4ca991d868a5643e4e73
Source noteuspto-grants-1998_04