Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133586Generated: October 26, 2026

1-Chloro-4-(chloromethyl)benzene → {[1-(4-Chlorobenzyl)piperidin-4-yl]methyl}amine

https://huagongshe.com/reaction/133586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Aminomethyl)piperidineHCID 23527—
SolventAcetonitrileHCID 6342—
Product{[1-(4-Chlorobenzyl)piperidin-4-yl]methyl}amineHCID 1842614569%

Reaction Conditions

Temperature60 °C

Reaction Steps

K2CO3 (3.02 g) and 4-chlorobenzyl chloride (3.52 g, 21.8 mmol) were successively added to an acetonitrile (100 mL) solution of 4-(aminomethyl)piperidine (7.00 g, 61.3 mmol). The resulting reaction mixture was stirred at 60° C. for 16 hours, cooled to 25° C. and concentrated. The obtained residue was fractionated between dichloromethane (75 mL) and water (50 mL) and then washed with water (50 mL×2) and brine (50 mL×1). The organic layer was dried (over MgSO4), concentrated and then purified by chromatography (SiO2, 4% H2O-iPrOH) to provide 4-(aminomethyl)-1-(4-chlorobenzyl)piperidine (3.58 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-f1d42b141bc340a0a10ca3237623865e
Source noteuspto-grants-2008_06