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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2309426Generated: November 3, 2026

4-Hydroxybenzaldehyde → Benzaldehyde, 4-(phenylmethoxy)-

https://huagongshe.com/reaction/2309426

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
SolventSodium chloride; waterHCID 57417360—
ProductBenzaldehyde, 4-(phenylmethoxy)-HCID 78109—

Reaction Steps

A solution of p-hydroxybenzaldehyde (3.66 g, 30 mmole) in dry DMF (20 ml) was stirred with anhydrous potassium carbonate (12.5 g, 90 mmole) and benzylbromide (6.16 g, 36 mmole) was added. After 18 hours, the mixture was diluted with brine (75 ml) and extracted three times with ether. The extracts were combined, washed with dilute brine, dried over anhydrous magnesium sulfate and evaporated in vacuo to afford a solid. Crystallization from ethyl ether in hexane gave 5 g of title E compound as light yellow flakes, with consistent spectral data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04695585
Source datasetuspto-grants-1987_09
ORD IDord-396adbcd24b6460589ad1f9b8830da35
Source noteuspto-grants-1987_09