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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982813Generated: October 29, 2026

beta-D-Glucose pentaacetate → HCID 12085573, compound

https://huagongshe.com/reaction/1982813

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/ethyl acetate=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 the 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 resulting 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 numberUS07541341B2
Source datasetuspto-grants-2009_06
ORD IDord-01b96ee83a8e41bb92ca70123e92b88b
Source noteuspto-grants-2009_06