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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28135Generated: October 25, 2026

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

https://huagongshe.com/reaction/28135

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 numberUS04225606
Source datasetuspto-grants-1980_09
ORD IDord-ba652881a6f84738800ac5379ff8ab49
Source noteuspto-grants-1980_09