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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 258785Erstellt: 25. Oktober 2026

4-(Aminomethyl)piperidine → 4-[2,4-Dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentylaminomethyl]piperidine

https://huagongshe.com/reaction/258785

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(Aminomethyl)piperidineHCID 23527—
Edukt2,4-Dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentanoneHCID 21425707—
EduktHCID 178418361HCID 178418361—
KatalysatorAdams' catalystHCID 345198—
LösungsmittelEthanolHCID 702—
Produkt4-[2,4-Dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentylaminomethyl]piperidineHCID 68123693—

Reaktionsschritte

A mixture of 2,4-dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentanone (g., 0.1 mole) and 4-aminomethylpiperidine (34.2 g., 0.3 mole) ml. ethanol is hydrogenated with PtO2 at room temperature and 40 psi hydrogen pressure. The 2.5 g. platinum catalyst is filtered off and the ethanol removed under reduced pressure. The residual oil is dissolved in ether and the ether solution washed several times with water to remove the excess 4-aminomethylpiperidine. The ether extracts are dried over anhydrous sodium sulfate and concentrated under vacuum to leave 4-[2,4-dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentylaminomethyl]piperidine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04033748
Quelldatensatzuspto-grants-1977_07
ORD IDord-ecd5d6c851ed49639d779e2f14a35b3b
Quellennotizuspto-grants-1977_07