Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066984Generated: November 2, 2026

N-(1-(Phenylmethyl)-4-piperidinyl)benzamide → N-4-Piperidylbenzamide

https://huagongshe.com/reaction/1066984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-(Phenylmethyl)-4-piperidinyl)benzamideHCID 40598—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductN-4-PiperidylbenzamideHCID 118120100%

Reaction Steps

To a suspension of 10% palladium on carbon (0.2 g) in 30 mL of ethyl alcohol was added a solution of 1-benzyl-4-benzamido-piperidine (0.5 g, 1.79 mmol) in ethyl alcohol (10 mL). The resulting suspension was hydrogenated at 100 psi at 50° C. for 30 h after which it was filtered through a pad of celite and the solvent was removed in vacuo to obtain 0.34 g (100%) of 4-benzamidopiperidine as a white solid. It was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06245773B1
Source datasetuspto-grants-2001_06
ORD IDord-2f29796371034863a69c1bad23542458
Source noteuspto-grants-2001_06