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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109985Generated: October 30, 2026

3,4-Dichlorobenzyl chloride → HCID 43130924, compound

https://huagongshe.com/reaction/2109985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichlorobenzyl chlorideHCID 7609—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Aminomethyl)piperidineHCID 23527—
SolventAcetonitrileHCID 6342—
ProductHCID 43130924HCID 43130924—

Reaction Conditions

Temperature60 °C

Reaction Steps

After dissolving 4-aminomethyl-piperidine (10 g) in acetonitrile (250 ml), 3,4-dichlorobenzyl chloride (5.8 g) and potassium carbonate (5 g) were added at room temperature, and the mixture was stirred at 60° C. overnight. The reaction mixture was filtered, the solvent was removed under reduced pressure, and the obtained residue was purified by thin-layer silica gel chromatography (dichloromethane/methanol/triethylamine=85/7/7) to obtain C-[1-(3,4-dichloro-benzyl)-piperidin-4-yl]-methylamine. The compound was identified by LC-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517875B2
Source datasetuspto-grants-2009_04
ORD IDord-7113bd673bd1425fb34e2734d68d0963
Source noteuspto-grants-2009_04