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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826623Generated: November 1, 2026

beta-D-Glucose pentaacetate → HCID 12085573, compound

https://huagongshe.com/reaction/1826623

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbeta-D-Glucose pentaacetateHCID 2724702—
ReactantHCID 12085536HCID 12085536—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 12085573HCID 1208557363.7%

Reaction Steps

To a suspension of ethyl (E)-3-[4-(2-hydroxybenzyl)phenyl]acrylate (0.34 g) and 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranose (1.4 g) in dichloromethane (3 mL) and toluene (9 ml) was added boron trifluoride-diethyl ether complex (0.45 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: hexane/ethylacetate=4/1) to give (E)-2-[4-(2-ethoxycarbonylvinyl)benzyl]phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside (0.47 g). To a solution of the obtained (E)-2-[4-(2-ethoxycarbonylvinyl)benzyl]phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside (0.46 g) in methanol (5 mL) was added sodium methoxide (0.010 g), 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: ethyl acetate) to give (E)-2-[4-(2-ethoxycarbonylvinyl)benzyl]phenyl β-D-glucopyranoside (0.31 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053060B2
Source datasetuspto-grants-2006_05
ORD IDord-1ffb3517eed54ddea40d454d60fe8ee6
Source noteuspto-grants-2006_05