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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706732Generated: October 30, 2026

Pyridine → HCID 23339068, compound

https://huagongshe.com/reaction/1706732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylacetyl chlorideHCID 7679—
ReactantHCID 23338990HCID 23338990—
SolventBenzeneHCID 241—
ProductHCID 23339068HCID 23339068—

Reaction Steps

To a stirred solution of 8 parts of ethyl 4-[(2,6-dimethylphenyl)amino]-1-piperidinecarboxylate in 4 parts of pyridine and 80 parts of benzene are added dropwise 7.7 parts of benzeneacetyl chloride in 40 parts of benzene. After the addition is complete, the whole is heated to reflux and stirred at reflux temperature for 3 h. 45. The reaction mixture is cooled and filtered. The benzene-phase is washed with water and then with sodium hydrogen carbonate solution and with water. After evaporation, an oily residue is obtained, which solidifies on triturating in 1,1'-oxybisethane, to yield 5 parts of ethyl 4-[N-(2,6-dimethylphenyl)-N-(phenylacetyl)amino]-1-piperidinecarboxylate; mp. 106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208418
Source datasetuspto-grants-1980_06
ORD IDord-b237897f4c894f55b341cac059ff6fbf
Source noteuspto-grants-1980_06