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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372448Generated: October 31, 2026

4-Hydroxybenzaldehyde → HCID 23397581, compound

https://huagongshe.com/reaction/1372448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2,3,4-Tri-O-acetylpentopyranosyl bromideHCID 11078288—
CatalystTetrabutylammonium BromideHCID 74236—
SolventDichloromethaneHCID 6344—
ProductHCID 23397581HCID 23397581—

Reaction Steps

p-Hydroxybenzaldehyde (2.2 g, 18 mmol), dichloromethane 18 mL, a 5% aqueous solution of sodium hydroxide (20 mL) were put in a 100 mL round bottom flask and stirred vigorously. At that time, the water phase turned yellow. To the resulting mixture, tetrabutylammonium bromide (1.0 g, 3.0 mmol) was added, and then a solution of 2,3,4-tri-O-acetyl-β-D-arabinopyranosyl bromide (4.0 g, 12 mmol) in dichloromethane (about 6 mL) was added dropwise. A reaction vessel was protected from light, and the resulting mixture was stirred vigorously at room temperature for 2 days. The separated organic phase was washed with 50 mL of a 5% aqueous solution of sodium hydroxide three times and then with 50 mL of water three times, dried over anhydrous sodium sulfate and evaporated to dryness to give the title compound. Light brown solid. Yield 1.9 g, 43%. The product was unstable at room temperature, and stored in the freezer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157432B2
Source datasetuspto-grants-2007_01
ORD IDord-ce3abdc5143d4d52a5300e6beff5898c
Source noteuspto-grants-2007_01