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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75840Generated: October 26, 2026

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

https://huagongshe.com/reaction/75840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzaldehydeHCID 126—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
ProductBenzaldehyde, 4-(phenylmethoxy)-HCID 78109—

Reaction Steps

To 4-Hydroxy benzaldehyde (10 g) in acetone (200 ml), potassium carbonate (16.96 g) was added and stirred. To this, benzyl bromide (12.67 ml) was added and the reaction mixture was refluxed for 3 hours and then cooled. The reaction mixture was filtered and the filtrate was concentrated to obtain pale brown colored oil which got solidified at room temperature. Solid was crystallized from DCM-Petroleum ether to obtain the title compound as pale yellow solid. Yield: 13 g (74%); 1HNMR (CDCl3; 300 MHz): δ 9.91 (s, 1H), 7.87 (d, 2H), 7.33-7.43 (m, 5H), 7.12 (d, 21-1) 5.17 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835428B2
Source datasetuspto-grants-2014_09
ORD IDord-4d56e7fd93da410b8bd0ac4a0d464ab6
Source noteuspto-grants-2014_09