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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737125Generated: October 31, 2026

4-Bromobenzoyl chloride → (4-Bromo-phenyl)-(3-phenyl-piperazin-1-yl)-methanone

https://huagongshe.com/reaction/737125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzoyl chlorideHCID 68515—
Reactant2-PhenylpiperazineHCID 250673—
SolventDichloromethaneHCID 6344—
Product(4-Bromo-phenyl)-(3-phenyl-piperazin-1-yl)-methanoneHCID 57849479—

Reaction Conditions

Temperature0 °C

Reaction Steps

This compound could be made in the following manner: 500 mg of 2-phenylpiperazine would be dissolved in dichloromethane and cooled to 0° C. A solution of 0.5 equiv. of 4-bromobenzoyl chloride in dichloromethane would be added dropwise over 1 h at 0° C. The reaction would be stirred at 0° C. for 0.5 h, then allowed to warm to room temperature and stirred for a further 3 h until complete conversion. The reaction mixture would be diluted with dichloromethane, washed with 1M aqueous sodium hydroxide solution and brine, then dried over sodium sulfate, filtered and concentrated in vacuo. The crude residue would be purified by column chromatography to afford (4-bromo-phenyl)-(3-phenyl-piperazin-1-yl)-methanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-9d7d4413c726459ea41f9b8dcbe5882c
Source noteuspto-grants-2009_09