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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28129Generated: October 28, 2026

Ethyl 4-[(2,6-dimethylphenyl)imino]-1-piperidinecarboxylate → HCID 23338990, compound

https://huagongshe.com/reaction/28129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-[(2,6-dimethylphenyl)imino]-1-piperidinecarboxylateHCID 23339012—
ReactantHCID 178418361HCID 178418361—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
ProductHCID 23338990HCID 23338990—

Reaction Steps

A mixture of 45 parts of ethyl 4-[(2,6-dimethylphenyl)-imino]-1-piperidinecarboxylate, 0.3 parts of platinum dioxide in 160 parts of methanol is hydrogenated at normal pressure and at a temperature between 24°and 35° C. After the calculated amount of hydrogen is taken up, hydrogenation is stopped. The catalyst is filtered off and the filtrate is evaporated. The oily residue is distilled, to yield 30 parts of the oily free base of ethyl 4-[(2,6-dimethylphenyl)amino]-1-piperidinecarboxylate; bp. 148°-153° C. at 0.01 mm. pressure. From this distillate, the hydrochloride salt is prepared in the usual manner in 1,1'-oxybisethane. The precipitated solid salt is filtered off and dried, yielding 28.5 parts of ethyl 4-[(2,6-dimethylphenyl)amino]-piperidinecarboxylate hydrochloride; mp. 195.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225606
Source datasetuspto-grants-1980_09
ORD IDord-8dbfba94f6d545ee8f3f3730a32c8d3b
Source noteuspto-grants-1980_09