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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49773Generated: October 26, 2026

4-Fluorobenzoyl chloride → N-(1-benzylpiperidin-4-yl)-4-fluorobenzamide

https://huagongshe.com/reaction/49773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzoyl chlorideHCID 67879—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
SolventDichloromethaneHCID 6344—
SolventDiisopropylethylamineHCID 81531—
ProductN-(1-benzylpiperidin-4-yl)-4-fluorobenzamideHCID 70250170.6%

Reaction Steps

To a solution of 1-benzyl-4-aminopiperidine (1.13 g) in dichloromethane (10 ml) were added a solution of 4-fluorobenzoyl chloride (0.99 g) in dichloromethane (1 ml) and diisopropylethylamine (1.09 ml) under cooling on an ice-water bath. The mixture was warmed to ambient temperature slowly under stirring. The mixture was diluted with dichloromethane and washed with water, saturated aqueous sodium hydrogen carbonate, water, and brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. A residue was purified by column chromatography (silica gel 100 ml, dichloromethane:methanol=15:1). After rinse with diisopropyl ether-n-hexane (1:1), N-(1-benzylpiperidin-4-yl)-4-fluorobenzamide (1.31 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-2a6f47bbdaae4925b1a064929ab38b76
Source noteuspto-grants-2004_03