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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835261Generated: October 29, 2026

Triethylamine → 3,4-dichlorobenzyl-4-piperidone

https://huagongshe.com/reaction/1835261

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 numberUS06770650B2
Source datasetuspto-grants-2004_08
ORD IDord-6741970a656945b29738014bb72cb437
Source noteuspto-grants-2004_08