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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 258785생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/258785

반응식

참여 물질

역할이름HCID투입량
반응물4-(Aminomethyl)piperidineHCID 23527—
반응물2,4-Dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentanoneHCID 21425707—
반응물HCID 178418361HCID 178418361—
촉매Adams' catalystHCID 345198—
용매EthanolHCID 702—
생성물4-[2,4-Dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentylaminomethyl]piperidineHCID 68123693—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04033748
출처 데이터셋uspto-grants-1977_07
ORD IDord-ecd5d6c851ed49639d779e2f14a35b3b
출처 메모uspto-grants-1977_07