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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372451Generated: November 3, 2026

4-Hydroxybenzaldehyde → HCID 23397582, compound

https://huagongshe.com/reaction/1372451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantSodium HydroxideHCID 14798—
Reactant2,3,4-Tri-O-acetyl-alpha-D-xylopyranosyl bromideHCID 11013202—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 23397582HCID 23397582—

Reaction Steps

p-Hydroxybenzaldehyde (2.2 g, 18 mmol), dichloromethane (20 mL) and a 5% aqueous solution of sodium hydroxide (25 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 dichloromethane (about 6 mL) solution of 2,3,4-tri-O-acetyl-α-D-xylopyranosyl bromide (4.0 g, 12 mmol) was added dropwise. The reaction vessel was protected from light. 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 1.5 g, 34%. 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-13c00cee9b83437db6e633f74ab9adc7
Source noteuspto-grants-2007_01