Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279291Erstellt: 24. Oktober 2026

1-Chloro-4-(chloromethyl)benzene → 3-Carbamoyl-1-(4-chlorobenzyl)piperidine

https://huagongshe.com/de/reaction/279291

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-4-(chloromethyl)benzeneHCID 7723—
EduktTriethylamineHCID 8471—
Edukt3-PiperidinecarboxamideHCID 92980—
EduktSodium BicarbonateHCID 516892—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-Carbamoyl-1-(4-chlorobenzyl)piperidineHCID 284579755,2%

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of nipecotamide (6.40 g, 50 mmol) in CH3CN (150 mL) and ethanol (20 mL) was treated with Et3N (7.0 mL, 50 mmol) and 4-chlorobenzyl chloride (8.05 g, 50 mmol). The reaction mixture was stirred at 50° C. for 16 h. After cooling to room temperature, saturated aqueous NaHCO3 (50 mL) and water (150 mL) was added to the reaction mixture. The mixture was extracted with ethyl acetate (150 mL×3) and the combined organic layers were washed with brine, dried (Na2SO4) and concentrated to give a pale red solid. The crude solid was washed with ether (100 mL) to afford 3-carbamoyl-1-(4-chlorobenzyl)piperidine (6.98 g, 54%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06362177B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-6c730d6f69b54ab6a3841806aca31ca0
Quellennotizuspto-grants-2002_03