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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254213Generated: October 29, 2026

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

https://huagongshe.com/reaction/2254213

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
ProductBenzaldehyde, 4-(phenylmethoxy)-HCID 7810994.6%

Reaction Steps

In 80 ml of dimethylformamide was dissolved 12.22 g of p-hydroxybenzaldehyde, and 17.66 g of anhydrous potassium carbonate and 13.0 ml of benzyl bromide were added to the solution and the mixture was stirred at room temperature in a nitrogen current for 1 hour. After the reaction, water was added to the reaction mixture and the formed precipitate was recovered by filtration and recrystallized from a dichloromethane/hexane mixed solvent to obtain 20.07 g (yield=94.6%) of 4-benzyloxybenzaldehyde in the form of a colorless needle.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05234951
Source datasetuspto-grants-1993_08
ORD IDord-6444889140ce4d5f991f163b2e7aa087
Source noteuspto-grants-1993_08