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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706731Generated: October 31, 2026

Phenylacetyl chloride → Ethyl 4-[(4-chlorophenyl)(phenylacetyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1706731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylacetyl chlorideHCID 7679—
ReactantEthyl 4-[(4-chlorophenyl)amino]piperidine-1-carboxylateHCID 2846949—
SolventBenzeneHCID 241—
ProductEthyl 4-[(4-chlorophenyl)(phenylacetyl)amino]piperidine-1-carboxylateHCID 3017393—

Reaction Steps

To a stirred solution of 58 parts of ethyl 4-[(4-chlorophenyl)amino]-1-piperidinecarboxylate in 240 parts of benzene is added dropwise a solution of 46.2 parts of benzeneacetyl chloride in 80 parts of benzene at a temperature between 40°-70° C. Upon completion, the whole is stirred and refluxed for 6 h. 15. The reaction mixture is cooled and filtered. The filtrate is washed successively with water, sodium hydrogen carbonate solution and water, then dried and evaporated in vacuo. The residue is crystallized from 1,1'-oxybisethane, yielding 47 parts of ethyl 4-[N-(4-chlorophenyl)-N-(phenylacetyl)amino]-1-piperidinecarboxylate; mp. 108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04208418
Source datasetuspto-grants-1980_06
ORD IDord-b2ff9329e4c54ec8b08f2cac505f4834
Source noteuspto-grants-1980_06