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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901505Generated: November 2, 2026

Water → 1-(3-Benzoylpropyl)-4-benzamidopiperidine

https://huagongshe.com/reaction/1901505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantN-4-PiperidylbenzamideHCID 118120—
Reactant4-ChlorobutyrophenoneHCID 253533—
SolventChloroformHCID 6212—
Product1-(3-Benzoylpropyl)-4-benzamidopiperidineHCID 100892549.1%

Reaction Steps

A mixture of 4-chlorobutyrophenone (447 mg, 2.45 mmol), 4-benzamidopiperidine (500 mg, 2.45 mmol) and K2CO3 (338 mg, 2.45 mmol) was heated up in boiling water bath for 1 hour. The reaction mixture was portioned between water and CHCl3. The organic layer was separated and dried over Na2SO4. After filtration and removal of solvent, the residue was purified by chromatography (SiO2, MeOH:CHCl3, 5:95). Recrystallization from AcOEt/hexane gave a white powder (78 mg, 8.2%). mp 143°-144° C.; 1H NMR (CD3OD, 400 MHz) δ 1.65 (dq, J1 =3.16 Hz, J2 =11.9 Hz, 2H), 1.90-2.00 (m, 4H), 2.18 (t, J=11.9 Hz, 2H), 2.48 (m, 2H), 3.00-3.10 (m, 4H), 3.88 (m, 1H), 7.40-8.00 (m, 10H); Mass spectrum (M+1)+ at m/z 351.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578611
Source datasetuspto-grants-1996_11
ORD IDord-5e93ab91a00f4d30badf3a7bf6aeadf3
Source noteuspto-grants-1996_11