Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230874Generated: October 26, 2026

beta-D-Galactose pentaacetate → 4-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyloxy)-3-(2-phenylethyl)benzofuran

https://huagongshe.com/reaction/230874

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbeta-D-Galactose pentaacetateHCID 94752—
Reactant4-Hydroxy-3-(2-phenylethyl)benzofuranHCID 23103521—
SolventDichloromethaneHCID 6344—
Product4-(2,3,4,6-tetra-O-acetyl-beta-D-galactopyranosyloxy)-3-(2-phenylethyl)benzofuranHCID 6713601549.5%

Reaction Steps

To a solution of 4-hydroxy-3-(2-phenylethyl)benzofuran (0.11 g) and 1,2,3,4,6-penta-O-acetyl-β-D-galactopyranose (0.37 g) in dichloromethane (5 mL) was added boron trifluoride-diethyl ether complex (0.12 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=3/1-3/2) to give 4-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyloxy)-3-(2-phenylethyl)benzofuran (0.13 g). This material was dissolved in methanol (5 mL). To the solution was added sodium methoxide (28% methanol solution, 0.043 mL), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1) to give the title compound (24 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566699B2
Source datasetuspto-grants-2009_07
ORD IDord-4c87c0f7e25f476eb12123bf1df46b81
Source noteuspto-grants-2009_07