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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300165Generated: November 1, 2026

4-Piperidinecarboxamide → 1-Benzylpiperidine-4-carboxamide

https://huagongshe.com/reaction/2300165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidinecarboxamideHCID 3772—
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
SolventDimethylformamideHCID 6228—
Product1-Benzylpiperidine-4-carboxamideHCID 78315649.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 15 g 4-piperidinecarboxamide, 16.3 g benzyl chloride, 32.3 g potassium carbonate and 200 ml N,N-dimethylformamide was stirred at 80° C. for 4 hr. The reaction solution was returned to room temperature, and aqueous sodium hydroxide was added thereto, and then it was extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and then evaporated. The resulting crystalline residue was washed with hexane/ethyl acetate and collected by filtration. 12.7 g of 1-benzyl-4-piperidine carboxamide was obtained as white flaky crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498159B1
Source datasetuspto-grants-2002_12
ORD IDord-a921b215a15c47868f05d77bb4efe194
Source noteuspto-grants-2002_12