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
Participants
| Role | Name | HCID | Charge |
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| Reactant | beta-D-Glucose pentaacetate | HCID 2724702 | — |
| Reactant | HCID 12085536 | HCID 12085536 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 12085573 | HCID 12085573 | 63.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07541341B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-01b96ee83a8e41bb92ca70123e92b88b |
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| Source note | uspto-grants-2009_06 |
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