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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264961Erstellt: 27. Oktober 2026

Acetyl chloride → n-Acetyl-4-(2-tert-butoxycarbonylaminoethyl)-piperidine

https://huagongshe.com/reaction/264961

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyl chlorideHCID 6367—
EduktTriethylamineHCID 8471—
Edukt4-(2-Aminoethyl)piperidine, 4-BOC protectedHCID 1501849—
LösungsmittelDichloromethaneHCID 6344—
Produktn-Acetyl-4-(2-tert-butoxycarbonylaminoethyl)-piperidineHCID 21458620—

Reaktionsschritte

0.5 g of 4-(2-tert-butoxycarbonylaminoethyl)-piperidine and 0.61 ml of triethylamine are dissolved in 5 ml of dichloromethane and, at 0° C., 0.22 ml of acetyl chloride is added. The reaction mixture is stirred at room temperature for 7 hours and then washed with water. The organic phase is concentrated by evaporation and purified by FC (10 g of silica gel, ethyl acetate/methanol=9:1). The title compound is obtained: Rf (ethyl acetate/methanol=9:1)=0.39.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646143
Quelldatensatzuspto-grants-1997_07
ORD IDord-295ad98eb0ea4cb9be882df9c54d9be6
Quellennotizuspto-grants-1997_07