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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679108Generated: November 1, 2026

4-(Aminomethyl)piperidine → HCID 70621136, compound

https://huagongshe.com/reaction/1679108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Aminomethyl)piperidineHCID 23527—
ReactantHCID 20363681HCID 20363681—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventEthanolHCID 702—
ProductHCID 70621136HCID 70621136—

Reaction Steps

A mixture of 2,4-dimethyl-1,5-di-(4-methylphenyl)-3-pentanone (29.4 g., 0.1 mole) and 4-aminomethylpiperidine (34.2 g., 0.3 mole) in 250 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-(4-methylphenyl)-3-pentylaminomethyl]piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04079059
Source datasetuspto-grants-1978_03
ORD IDord-a490d07c5f154432a8ab8230e0c21481
Source noteuspto-grants-1978_03