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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483483Generated: October 30, 2026

Acetic Acid → N-(1-benzoyl-4-piperidinyl)-2-(2-carbamoylethyl)aniline

https://huagongshe.com/reaction/483483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantN-Benzoyl-4-piperidoneHCID 90583—
Reactant2-AminobenzenepropanamideHCID 19031234—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
ProductN-(1-benzoyl-4-piperidinyl)-2-(2-carbamoylethyl)anilineHCID 19031102—

Reaction Steps

2-(2-Carbamoylethyl)aniline (37 g) and 1-benzoyl-4-oxopiperidine (67.6 g) are dissolved in ethanol (500 ml) and to the solution is added acetic acid to adjust the pH of the solution to about 5.5. To the solution is further added PtO2 (1 g) and the mixture is stirred under 1 atm. at room temperature under H2 atmosphere. When H2 is absorbed up to 5 liters, the reaction is stopped and the catalyst is separated by filtration. The filtrate is concentrated to give N-(1-benzoyl-4-piperidinyl)-2-(2-carbamoylethyl)aniline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225402
Source datasetuspto-grants-1993_07
ORD IDord-a597d6581fb643beb34b8b2696414c64
Source noteuspto-grants-1993_07