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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610444Generated: November 1, 2026

Water → Phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-(4-methoxybenzyl)-1-thio-beta-D-glucopyranoside

https://huagongshe.com/reaction/610444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant4-Azido-3-chlorobenzyl bromideHCID 11482000—
ReactantPhenyl 2,3,4-tri-O-(4-methoxybenzyl)-1-thio-beta-D-glucopyranosideHCID 15433386—
SolventDimethylformamideHCID 6228—
ProductPhenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-(4-methoxybenzyl)-1-thio-beta-D-glucopyranosideHCID 1543338779.1%

Reaction Steps

To a solution of phenyl 2,3,4-tri-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (8) (1.25 g, 1.98 mmol) and 4-azido-3-chlorobenzyl bromide (584 mg, 2.37 mmol) in DMF (10 ml) was added sodium hydride (60% in oil, 95 mg, 2.37 mmol), and the resulting mixture was stirred at room temperature for 3 hr. Cold water was added and the mixture was extracted twice with ether. The combined ether layers were washed with water and saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue obtained was purified by silica gel column chromatography (eluent; hexane:ethyl acetate=4:1) to give phenyl 6-O-(4-azido-3-chlorobenzyl)-2,3,4-tri-O-(4-methoxybenzyl)-1-thio-β-D-glucopyranoside (9) as white crystals (1.25 g, yield 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998595
Source datasetuspto-grants-1999_12
ORD IDord-43b604fd80b34958b88a63bb8a57dd36
Source noteuspto-grants-1999_12