HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982829Generated: October 28, 2026
beta-D-Glucose pentaacetate → HCID 12085619, compound
https://huagongshe.com/reaction/1982829
Participants
| Role | Name | HCID | Charge |
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| Reactant | beta-D-Glucose pentaacetate | HCID 2724702 | — |
| Reactant | HCID 21909273 | HCID 21909273 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 12085619 | HCID 12085619 | — |
Reaction Steps
To a suspension of 4-(2-hydroxybenzyl)benzamide (0.063 g) and 1,2,3,4,6-penta-O-acetyl-β-D-glucopyranose (0.33 g) in toluene (3 mL) was added boron trifluoride diethyl ether complex (0.11 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 2-(4-carbamoylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside. To a solution of the obtained 2-(4-carbamoylbenzyl)phenyl 2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside in methanol (5 mL) was added sodium methoxide (0.005 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/ethanol=5/1) to give 2-(4-carbamoylbenzyl)phenyl β-D-glucopyranoside (0.068 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-93557f1a7ad84819be3c195b522ea7df |
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| Source note | uspto-grants-2009_06 |
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