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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115637Generated: November 1, 2026

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

https://huagongshe.com/reaction/2115637

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 numberUS07435743B2
Source datasetuspto-grants-2008_10
ORD IDord-9ae1269b4ac9473e95a964343d4859e7
Source noteuspto-grants-2008_10