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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632242Generated: November 1, 2026

4'-Hydroxyacetophenone → 1-[4-(2-Phenylethoxy)phenyl]ethanone

https://huagongshe.com/reaction/1632242

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-HydroxyacetophenoneHCID 7469—
ReactantPhenethyl bromideHCID 7666—
ReactantPotassium CarbonateHCID 11430—
SolventAcetoneHCID 180—
Product1-[4-(2-Phenylethoxy)phenyl]ethanoneHCID 13340057—

Reaction Steps

A stirred mixture of 18.5 g. of phenethylbromide, 20.4 g. of p-hydroxyacetophenone, 17.3 g. of anhydrous potassium carbonate and 150 ml. of acetone was refluxed under argon for 22 hours. The reaction was then cooled and partitioned between ether and water. The ether layer was washed with water and then extracted with two 100 ml. portions of cold 1N sodium hydroxide. These extracts were combined, washed with water and brine, dried and evaporated to an oil. The oil was purified by chromatography, giving the desired intermediate as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04474809
Source datasetuspto-grants-1984_10
ORD IDord-b6f6c19a5129447787131047731252e0
Source noteuspto-grants-1984_10