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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322027Generated: October 31, 2026

Phenacyl bromide → 2-(2-Bromophenoxy)-1-phenylethan-1-one

https://huagongshe.com/reaction/322027

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant2-BromophenolHCID 7244—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product2-(2-Bromophenoxy)-1-phenylethan-1-oneHCID 3016354—

Reaction Steps

To a solution of 2-bromophenol (8.71 g; 50.3 mmol) and bromoacetophenone (10.1 g; 50.5 mmol) in 50 ml acetone was added K2CO3 (7.02 g; 50.8 mmol). The mixture was heated to reflux for 10 h, cooled to r.t., filtered, diluted with EtOAc (100 ml), washed with HCl (1.0 M, 2×100 ml) and brine, dried over MgSO4 and concentrated. The residual solid was recrystallized from EtOAc:hexane to afford the desired material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211197B1
Source datasetuspto-grants-2001_04
ORD IDord-e8ea565d4667442bad8a8029ce85b129
Source noteuspto-grants-2001_04