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HRID 1415332Erstellt: 26. Oktober 2026

Acrylonitrile → 1-(3-Aminopropyl)-4-[2-(1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]-3-pentylamino)ethyl]piperidine

https://huagongshe.com/reaction/1415332

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcrylonitrileHCID 7855—
Edukt4-PiperidineethanamineHCID 1512602—
Edukt1,5-Di-(3,3-dimethylnorborn-2-yl)-3-pentanoneHCID 21332846—
Produkt1-(3-Aminopropyl)-4-[2-(1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]-3-pentylamino)ethyl]piperidineHCID 21483969—

Reaktionsschritte

As an alternative to obtaining a mixture of Schiff bases VI and VI(a) or VI(b), the reaction can be conducted stepwise. For example, 4-(2-aminoethyl)piperidine may be converted to a Schiff base with 1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]pentan-3-one, catalytically reduced, the ring nitrogen selectively cyanoethylated with acrylonitrile, followed by catalytic hydrogenation to furnish 1-(3-aminopropyl)-4-[2-(1,5-di-[3,3-dimethylbicyclo[2.2.1]hept-2-yl]-3-pentylamino)ethyl]piperidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04003934
Quelldatensatzuspto-grants-1977_01
ORD IDord-71023bb448a74992ad683619ac9ef9d1
Quellennotizuspto-grants-1977_01