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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26742Generated: October 25, 2026

Triethylamine → ethyl 4-{N-(4-chlorophenyl)-N-[(4-methoxyphenyl)acetyl]amino}-1-piperidinecarboxylate

https://huagongshe.com/reaction/26742

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Methoxyphenylacetyl chlorideHCID 2734688—
ReactantEthyl 4-[(4-chlorophenyl)amino]piperidine-1-carboxylateHCID 2846949—
SolventBenzeneHCID 241—
Productethyl 4-{N-(4-chlorophenyl)-N-[(4-methoxyphenyl)acetyl]amino}-1-piperidinecarboxylateHCID 23339060—

Reaction Steps

To a stirred solution of 15 parts of ethyl 4-[(4-chlorophenyl)-amino]-1-piperidinecarboxylate, 5.4 parts of N,N-diethylethanamine and 160 parts of benzene is added dropwise 11.07 parts of 4-methoxybenzeneacetyl chloride at a temperature between 32° to 40° C. After the addition is complete, the whole is stirred and refluxed for 3 hours. The reaction mixture is cooled and filtered. The filtrate is washed successively with water, sodium hydrogen carbonate solution and water, dried, filtered and evaporated in vacuo. The oily residue is crystallized from a mixture of 56 parts of 1,1'-oxybisethane and 40 parts of hexane. The crude solid product is filtered off and recrystallized from a mixture of benzene and 1,1'-oxybisethane, yielding 3 parts of ethyl 4-{N-(4-chlorophenyl)-N-[(4-methoxyphenyl)acetyl]amino}-1-piperidinecarboxylate; mp. 137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151286
Source datasetuspto-grants-1979_04
ORD IDord-fb35e9fe41e5429aa950f28afde72766
Source noteuspto-grants-1979_04