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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246927Generated: October 30, 2026

N-(1-Benzyl-piperidin-3-yl)-N-phenyl-propionamide → N-phenyl-N-piperidin-3-yl-propionamide

https://huagongshe.com/reaction/1246927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(1-Benzyl-piperidin-3-yl)-N-phenyl-propionamideHCID 12741868—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductN-phenyl-N-piperidin-3-yl-propionamideHCID 1274186997.2%

Reaction Steps

A mixture of N-(1-benzyl-piperidin-3-yl)-N-phenyl-propionamide (165) (150 mg) and Pd—C(10%, 50 mg) and MeOH (50 ml) was stirred under H2 (1 atm) for 24 hr. The catalyst was removed by filtration through Celite to give 166 as a colorless oil (105 mg, 97%). 1H-NMR (300 MHz, CDCl3) δ 7.41 (m, 3H), 7.10 (m, 2H), 3.20 (m 1H), 2.90 (m, 1H), 2.40–2.20 (m, 2H), 1.90 (m, 2H), 1.60 (m, 4H), 1.20 (m, 1H), 1.00 (t, 3H) ppm; LRMS (calculated for C14H21N2O) (M+1)+ 233. found 233.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129228B2
Source datasetuspto-grants-2006_10
ORD IDord-06f94b1807d84efb91598db626ad20a9
Source noteuspto-grants-2006_10