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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964863Generated: October 25, 2026

Benzyl Alcohol → Benzyl 2,3,4-tri-O-acetyl-alpha-D-lyxopyranoside

https://huagongshe.com/reaction/964863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
Reactant2,3,4-tri-O-acetyl-alpha-lyxopyranosyl bromideHCID 13048893—
ReactantCyanide mercuryHCID 14367217—
CatalystMercury bromideHCID 24830—
SolventAcetonitrileHCID 6342—
ProductBenzyl 2,3,4-tri-O-acetyl-alpha-D-lyxopyranosideHCID 6763832096.1%

Reaction Steps

A solution of compound 2 (21 g, 61.9 mmol) in acetonitrile (200 ml) and benzyl alcohol (9.6 ml, 92.3 mmol) was vigorously stirred with molecular sieves (4 Å, 25 g), mercury bromide (25 g, 69.4 mmol), mercury cyanide (18.2 g, 12.0 mmol) under argon for 18 hours. The organic layer was filtered through celite and diluted with dichloromethane (250 ml) which was washed with water, aq. NaHCO3 and aq. NaCl and dried (Na2 SO4). The solvent was filtered and then evaporated under reduced pressure. The syrupy residue was chromatographed on silica gel (filter technique) using 1.5:1 hexane-ethyl acetate to give 3 (21.8 g, 90.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05773239
Source datasetuspto-grants-1998_06
ORD IDord-d563b2c918d148debb74d76c47142d92
Source noteuspto-grants-1998_06