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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224118Generated: November 2, 2026

Piperazine → 1-((4-Chlorophenyl)(1-methylpiperidin-4-yl)methyl)piperazine

https://huagongshe.com/reaction/2224118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Chloro(4-chlorophenyl)methyl)-1-methylpiperidineHCID 59716933—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-((4-Chlorophenyl)(1-methylpiperidin-4-yl)methyl)piperazineHCID 5971693762%

Reaction Steps

A mixture of 4-(chloro(4-chlorophenyl)methyl)-1-methylpiperidine (1.2 g, 4.66 mmol) in butanone (10 ml), anhydrous piperazine (1.58 g, 18.45 mmol), anhydrous K2CO3 (0.63 g, 4.61 mmol) and KI (0.76 g, 4.61 mmol) was refluxed under nitrogen for 18 hours. The mixture was then cooled and filtered and the solvent removed in vacuo. The residue was dissolved in CH2Cl2 (50 ml) and washed with water (30 ml). Drying and removal of the solvent followed by chromatography (CH2Cl2:CH3OH:NH4OH 90:10:0.5) afforded desired product in 62% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378420B2
Source datasetuspto-grants-2008_05
ORD IDord-99f61c6a5c9b48fb9a0627fe3bbf3435
Source noteuspto-grants-2008_05