Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 737145Generated: October 25, 2026

4-Bromobenzyl bromide → 1-(4-Bromo-benzyl)-3-isopropyl-piperazine

https://huagongshe.com/reaction/737145

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromobenzyl bromideHCID 68527—
Reactant2-(Propan-2-yl)piperazineHCID 558976—
SolventAcetonitrileHCID 6342—
Product1-(4-Bromo-benzyl)-3-isopropyl-piperazineHCID 57849456—

Reaction Conditions

Temperature0 °C

Reaction Steps

0.7 g of 2-isopropyl-piperazine could be dissolved in acetonitrile and cooled to 0° C. A solution of 0.5 quiv. 4-bromobenzylbromide in acetonitrile could be added dropwise over 1 h. The reaction would be stirred at room temperature for 2 h. The reaction mixture could be concentrated and the residue could be purified by column chromatography (silica, eluent dichloromethane, 0-5% methanol, 0-0.5% dimethylethylamine) to afford 1-(4-bromo-benzyl)-3-isopropyl-piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595397B2
Source datasetuspto-grants-2009_09
ORD IDord-ab84154b14f74b55ad5a7dce6f1af402
Source noteuspto-grants-2009_09