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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973456Generated: October 31, 2026

Water → Cyclohexanone, 2-[2-(4-bromophenyl)-2-oxoethyl]-

https://huagongshe.com/reaction/1973456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
Reactant4-Bromophenacyl bromideHCID 7454—
Reactant1-Pyrrolidino-1-cyclohexeneHCID 70768—
ProductCyclohexanone, 2-[2-(4-bromophenyl)-2-oxoethyl]-HCID 12270330—

Reaction Steps

A suspension of 50 g (0.18 mole) of p-bromophenacyl bromide in 215 ml. of toluene is added in small portions to a stirred boiling solution of 27.2 g (0.18 mole) of 1-pyrrolidino-1-cyclohexene in 90 ml. of toluene. The mixture is heated under reflux for 2 hours, diluted with 90 ml. of water and refluxed for 3 hours. The layers are separated and the aqueous phase is extracted with ether. The organic solution is dried over sodium sulfate and concentrated to an oil which solidifies. The solid is recrystallized from a cyclohexane-ethanol mixture to give 2-(p-bromophenacyl)-cyclohexanone as colorless crystals, m.p. 78°-80° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03997557
Source datasetuspto-grants-1976_12
ORD IDord-2e639a9348ad4c82a41a95c86382af2d
Source noteuspto-grants-1976_12