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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133583Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/133583

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

Triethylamine (7.0 mL, 50 mmol) and 4-chlorobenzyl chloride (8.05 g, 50 mmol) were added to a solution of nipecotamide (6.40 g, 50 mmol) in acetonitrile (150 mL) and ethanol (20 mL). The resulting reaction mixture was stirred at 50° C. for 16 hours and cooled to room temperature. A saturated aqueous solution of NaHCO3 (50 mL) and water (150 mL) were then added, and the resulting mixture was extracted with ethyl acetate (150 mL×3). The extracts were washed with brine, dried over Na2SO4 and concentrated to afford a light-red solid. The obtained crude solid was washed with ether (100 mL) to provide 3-carbamoyl-1-(4-chlorobenzyl)piperidine (6.98 g, 54%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390830B1
Quelldatensatzuspto-grants-2008_06
ORD IDord-6f4b2841fe374baeadbc5ec0cd15c8f0
Quellennotizuspto-grants-2008_06