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HRID 258785作成日:2026年10月27日

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

https://huagongshe.com/reaction/258785

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Aminomethyl)piperidineHCID 23527—
反応物2,4-Dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentanoneHCID 21425707—
反応物HCID 178418361HCID 178418361—
触媒Adams' catalystHCID 345198—
溶媒EthanolHCID 702—
生成物4-[2,4-Dimethyl-1,5-di-(3,3-dimethylnorborn-2-yl)-3-pentylaminomethyl]piperidineHCID 68123693—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04033748
出典データセットuspto-grants-1977_07
ORD IDord-ecd5d6c851ed49639d779e2f14a35b3b
出典メモuspto-grants-1977_07