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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129078Generated: October 25, 2026

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

https://huagongshe.com/reaction/129078

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperonylamineHCID 2723901—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Chlorobenzoyl)piperidin-4-oneHCID 1523140474.6%

Reaction Steps

87.5 g of 4-chlorobenzoyl chloride and a solution of 276 g of potassium carbonate in 552 ml of water cooled to 5° C. are added successively with stirring to a suspension of 80.6 g of powdered 4-piperidone hydrochloride hydrate in 1 l of tetrahydrofuran. The mixture is stirred at ambient temperature for a further 45 minutes. The organic phase is then separated off, the aqueous phase is extracted twice more with ethyl acetate, and the organic phases are combined, dried and evaporated down. The residue is dissolved in ethyl acetate and the solution is treated with petroleum ether. 88.6 g of the title compound of melting point 61°-63° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05466687
Source datasetuspto-grants-1995_11
ORD IDord-6d7f17500ad642cb9fadff2d9312fea8
Source noteuspto-grants-1995_11