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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840752Generated: October 31, 2026

Triethylamine → 3,4-dichlorobenzyl-4-piperidone

https://huagongshe.com/reaction/1840752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Bromomethyl)-1,2-dichlorobenzeneHCID 639726—
Reactant4-Piperidone hydrochlorideHCID 3084851—
SolventEthanolHCID 702—
Product3,4-dichlorobenzyl-4-piperidoneHCID 1084877681.9%

Reaction Steps

To a suspension of 4-piperidone hydrochloride (3.52 g, 22.9 mmol) in ethanol (40 ml) was added triethylamine (10.8 ml, 91.6 mmol), followed by the addition of 3,4-dichlorobenzyl bromide (5.0 g, 20.8 mmol) and the reaction mixture was stirred overnight at room temperature. The reaction mixture was concentrated in vacuo and the residue was partitioned between water and ethyl acetate. The ethyl acetate layer was separated, washed with brine, dried over magnesium sulfate and concentrated in vacuo. Column chromatography with 25% ethyl acetate and 25% dichloromethane in hexanes gave 1-(3,4-dichlorobenzyl)-4-piperidone (4.4 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683074B1
Source datasetuspto-grants-2004_01
ORD IDord-efb15d97742d441bb952f6adeea08577
Source noteuspto-grants-2004_01