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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394559Generated: October 29, 2026

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

https://huagongshe.com/reaction/394559

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) δ1.65 (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 numberUS06602888B2
Source datasetuspto-grants-2003_08
ORD IDord-2c57d1872ace47f39f7aa6e63e33559d
Source noteuspto-grants-2003_08