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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968441Generated: October 29, 2026

4-Hydroxybenzaldehyde → HCID 23397582, compound

https://huagongshe.com/reaction/968441

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, a 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. A 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 numberUS06958389B2
Source datasetuspto-grants-2005_10
ORD IDord-eb16844ebd1546b9897f4b2dcf002900
Source noteuspto-grants-2005_10