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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26741Generated: October 29, 2026

Pyridine → HCID 23339068, compound

https://huagongshe.com/reaction/26741

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 3h. 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 numberUS04151286
Source datasetuspto-grants-1979_04
ORD IDord-37c6f292c96845a9b52d30991246307e
Source noteuspto-grants-1979_04