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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611113Generated: October 29, 2026

Benzyl Bromide → 1-[2-(Benzyloxy)phenyl]ethan-1-one

https://huagongshe.com/reaction/1611113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant2'-HydroxyacetophenoneHCID 8375—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product1-[2-(Benzyloxy)phenyl]ethan-1-oneHCID 52051388%

Reaction Steps

A mixture of 2′-hydroxyacetophenone (68.1 g, 0.500 mol), benzylbromide (94.1 g, 0.550 mol) and K2CO3 (103 g, 0.750 mol) in acetone (1.0 L) was heated at reflux, and the stirring was continued overnight. After cooled to room temperature, the mixture was concentrated under reduced pressure. The residue was diluted with water, and extracted with ethyl acetate. The separated organic phase was washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The crude product was purified by distillation under reduced pressure to give 1-[2-(benzyloxy)phenyl]ethanone as a colorless oil. (100 g, yield; 88%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-719eb814374d468eb30a8f86c4f44fcd
Source noteuspto-grants-2006_01