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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294441Generated: October 25, 2026

Benzyl Bromide → 2,3,4,6-Tetra-O-benzyl-alpha-D-galactopyranosyl Fluoride

https://huagongshe.com/reaction/1294441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactantalpha-D-galactosyl fluorideHCID 10921145—
CatalystSilver(II) oxideHCID 92152—
SolventDimethylformamideHCID 6228—
Product2,3,4,6-Tetra-O-benzyl-alpha-D-galactopyranosyl FluorideHCID 9959029—

Reaction Conditions

Temperature-20 °C

Reaction Steps

α-D-galactopyranosyl fluoride (2.30 g, 12.62 mmol) was dissolved in dry DMF (40 ml) and, at −20° C., benzyl bromide (12.95 g, 75.72 mmol) and silver oxide (10 g) were added. The reaction mixture was stirred at −20° C. for 5 h and then at room temperature for 24 h. The salts were then filtered off and the filtrate was evaporated in vacuo. The residue was purified by column chromatography on silica gel (350 g) with 15:1 petroleum ether/ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241595B2
Source datasetuspto-grants-2007_07
ORD IDord-75f8de51bba34535985917060252b27d
Source noteuspto-grants-2007_07