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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 4-[(2,6-dimethylphenyl)imino]-1-piperidinecarboxylate | HCID 23339012 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Adams' catalyst | HCID 345198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23338990 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225606 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-8dbfba94f6d545ee8f3f3730a32c8d3b |
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| Source note | uspto-grants-1980_09 |
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