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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102324Generated: November 1, 2026

Sodium Hydroxide → HCID 57802353, compound

https://huagongshe.com/reaction/2102324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactantalpha-D-Glucopyranosyl bromide, tetraacetateHCID 101776—
ReactantHCID 23079532HCID 23079532—
SolventDichloromethaneHCID 6344—
ProductHCID 57802353HCID 5780235386.6%

Reaction Steps

To a suspension of 4-benzyl-1,5-diisopropyl-1,2-dihydro-3H-pyrazole-3-one (0.078 g), acetobromo-α-D-glucose (0.62 g) and benzyl (n-tributyl)ammonium bromide (0.054 g) in dichioromethane (4 mL) was added a sodium hydroxide aqueous solution (5 mol/L, 0.6 mL) and the mixture was stirred at room temperature for 2 hours. The reaction mixture was purified by column chromatography on aminopropylated silica gel (eluent: tetrahydrofuran). The obtained semi purified 4-benzyl-1,5diisopropyl-3-(2,3,4,6-tetraacetyl-1β-D-glucopyranosyloxy)-1H-pyrazole was dissolved in methanol (3 mL), and sodium methoxide (28% methanol solution, 0.58 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 the residue was acidified by adding 10% citric acid aqueous solution. The mixture was purified by solid phase extraction on ODS (washing solvent: water, eluent: methanol). Further purification by column chromatography on silica gel (eluent: dichloromethane/methanol=10/1) gave the title compound (0.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576063B2
Source datasetuspto-grants-2009_08
ORD IDord-740e5c5de6c94182bef79747846e0a45
Source noteuspto-grants-2009_08