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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28133Generated: October 26, 2026

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

https://huagongshe.com/reaction/28133

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 6h.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 numberUS04225606
Source datasetuspto-grants-1980_09
ORD IDord-d0e8775e28bf4a14b64ab3c30fe80e8a
Source noteuspto-grants-1980_09