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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829181Generated: November 2, 2026

N-(1-Benzyl-4-phenylpiperidin-4-YL)acetamide → N-(4-Phenylpiperidin-4-yl)acetamide

https://huagongshe.com/reaction/1829181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-Benzyl-4-phenylpiperidin-4-YL)acetamideHCID 18964199—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductN-(4-Phenylpiperidin-4-yl)acetamideHCID 15886675—

Reaction Steps

A mixture of N-(1-Benzyl-4-phenyl-4-piperidinyl)acetamide (Bioorg. Med. Chem. Lett. 1996; 6(19); 2307) (49 g, 158 mmol), and palladium hydroxide (5 g) in methanol (600 ml) was hydrogenated at 50 psi and room temperature for 18 hours. The mixture was filtered, the filtrate concentrated under reduced pressure and the residue azeotroped with dichloromethane to give the title compound as a foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060836B2
Source datasetuspto-grants-2006_06
ORD IDord-3f9a95e0015e442391fdeb845217494e
Source noteuspto-grants-2006_06