Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251760Generated: October 25, 2026

p-Bromoacetophenone → 2-(4-Bromophenyl)quinoline

https://huagongshe.com/reaction/251760

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-BromoacetophenoneHCID 7466—
ReactantSodium HydroxideHCID 14798—
Reactant2-AminobenzophenoneHCID 76080—
SolventEthanolHCID 702—
Product2-(4-Bromophenyl)quinolineHCID 147344478.3%

Reaction Steps

Dissolving 5.0 g (25 mmol) of 4-bromoacetophenone and 5.0 g (25 mmol) of 2-aminobenzophenon into 50 milliliter of ethanol, adding 3.1 g of sodium hydroxide, the resultant suspension was refluxed under heating for 7 hours. After completion of the reaction, separation with filtration was carried out and resultant crystals were washed with water and ethanol, thereby obtaining 5.56 g of 2-(4-bromo-phenyl)-quinoline (yield: 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07867629B2
Source datasetuspto-grants-2011_01
ORD IDord-c554a8b419c44fce967ba6f31283fd67
Source noteuspto-grants-2011_01