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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 457513Generated: October 26, 2026

alpha-D-Glucopyranosyl bromide, tetraacetate → 4-[(4-Ethylphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxy)-1H-pyrazole

https://huagongshe.com/reaction/457513

Reaction equation

Participants

RoleNameHCIDCharge
Reactantalpha-D-Glucopyranosyl bromide, tetraacetateHCID 101776—
Reactant1,2-dihydro-4-(4-ethylbenzyl)-5-methyl-3H-pyrazol-3-oneHCID 11984072—
CatalystHCID 178418647HCID 178418647—
SolventTetrahydrofuranHCID 8028—
Product4-[(4-Ethylphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-beta-D-glucopyranosyloxy)-1H-pyrazoleHCID 6733557838.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a suspension of 4-[(4-ethylphenyl)methyl]-5-methyl-1,2-dihydro-3H-pyrazol-3-one (0.65 g) and acetobromo-α-D-glucose (1.2 g) in tetrahydrofuran (15 mL) was added silver carbonate (0.83 g), and the mixture was stirred at 60° C. overnight under light shielding. The reaction mixture was purified by column chromatography on aminopropyl silica gel (eluent: tetrahydrofuran), and successively by column chromatography on silica gel (eluent: hexane/ethyl acetate=1/3) to give 4-[(4-ethylphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole (0.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189702B2
Source datasetuspto-grants-2007_03
ORD IDord-80191eb713a3491e9f19c7bd5944fa19
Source noteuspto-grants-2007_03