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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49773Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/49773

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Fluorobenzoyl chlorideHCID 67879—
Edukt1-Benzyl-4-piperidylamineHCID 415852—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelDiisopropylethylamineHCID 81531—
ProduktN-(1-benzylpiperidin-4-yl)-4-fluorobenzamideHCID 70250170,6%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710043B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-2a6f47bbdaae4925b1a064929ab38b76
Quellennotizuspto-grants-2004_03