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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601901Generated: October 30, 2026

4-Piperidinecarboxamide → 1-Benzylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1601901

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-PiperidinecarboxamideHCID 3772—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
SolventDimethylformamideHCID 6228—
Product1-Benzylpiperidine-4-carboxamideHCID 78315662.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

85.5 g of benzyl bromide are added dropwise at RT to a mixture of 58.2 g of isonipecotamide and 69 g of K2CO3 in 275 ml of DMF and the reaction mixture is stirred for 2 hours at 50° C. It is concentrated under vacuum, the residue is taken up with water and extracted with DCM, the organic phase is washed with water and dried over Na2SO4 and the solvent is evaporated off under vacuum to give 62 g of the expected product after crystallization from 300 ml of water and drying under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05977359
Source datasetuspto-grants-1999_11
ORD IDord-d2d63158243a4cbd8d9c4c5b439d620f
Source noteuspto-grants-1999_11