Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704408Generated: November 1, 2026

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

https://huagongshe.com/reaction/1704408

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 numberUS04126689
Source datasetuspto-grants-1978_11
ORD IDord-56cebca10bc74200b2cc951edb988cb0
Source noteuspto-grants-1978_11