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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102325Generated: November 1, 2026

Sodium Hydroxide → HCID 57802341, compound

https://huagongshe.com/reaction/2102325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantalpha-D-Glucopyranosyl bromide, tetraacetateHCID 101776—
ReactantHCID 66971382HCID 66971382—
SolventDichloromethaneHCID 6344—
ProductHCID 57802341HCID 5780234161.2%

Reaction Steps

To a suspension of 4-[(4-isobutylphenyl)methyl]-5-isopropyl-1,2-dihydro-3H-pyrazole-3-one (0.082 g), acetobromo-α-D-glucose (0.62 g) and benzyl(n-tributyl)ammonium bromide (0.054 g) in dichloromethane (3 mL) was added a sodium hydroxide aqueous solution (5 mol/L, 0.9 mL), and the mixture was stirred at room temperature overnight. The reaction mixture was purified by column chromatography on aminopropylated silica gel (eluent:tetrahydrofuran). The obtained semi purified 5-isopropyl-4-[(4-isobutylphenyl)methyl]-3-(2,3,4,6-tetraacetyl-β-D-glucopyranosyloxy)-1H-pyrazole was dissolved in methanol (5 mL), and sodium methoxide (28% methanol solution, 0.29 mL) was added to the solution. The mixture was stirred at room temperature for 2 hours. The solvent of the reaction mixture was removed under reduced pressure, and water was added to the residue. The mixture was purified by solid phase extraction (washing solvent:water, eluent:methanol). Further purification by column chromatography on silica gel (eluent:dichloromethane/methanol=20/1-7/1) gave the title compound (0.080 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576063B2
Source datasetuspto-grants-2009_08
ORD IDord-3202dfe70e46493a90efccfe6f96c018
Source noteuspto-grants-2009_08