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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552327Generated: October 31, 2026

Triethylamine → 1-(4-Chlorobenzoyl)piperidin-4-one

https://huagongshe.com/reaction/552327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantPotassium HydroxideHCID 14797—
ReactantPiperidin-2-one--hydrogen chloride (1/1)HCID 20088740—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product1-(4-Chlorobenzoyl)piperidin-4-oneHCID 15231404—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Triethylamine (4.4 g, 43.0 mmol) and a catalytic amount of DMAP were added to a solution of piperidone hydrochloride (3.0 g, 19.5 mmol) in CH2Cl2 (20 ml). After cooling to −10° C., 4-chlorobenzoyl chloride (3.8 g, 21.5 mmol) dissolved in CH2Cl2 (10 ml) was slowly added and the mixture was stirred at RT for 16 h. 5M potassium hydroxide solution (20 ml) was added to the suspension, the organic phase was separated off and the aqueous phase was extracted with CH2Cl2 (3×10 ml). After drying of the combined organic phases over Na2SO4, filtration and removal of the solvent, the product 1-(4-chlorobenzoyl)piperidin-4-one was obtained in a yield of 4.4 g (95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951815B2
Source datasetuspto-grants-2011_05
ORD IDord-87c0fc6e837843ed8d545f17ddb2f652
Source noteuspto-grants-2011_05