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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28151Generated: October 25, 2026

Triethylamine → N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride

https://huagongshe.com/reaction/28151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-IodopropaneHCID 33643—
ReactantN-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamideHCID 162188—
SolventBenzeneHCID 241—
ProductN-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochlorideHCID 23339041—

Reaction Steps

To a stirred solution of 4 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide and 3 parts of N,N-diethylethanamine in 200 parts of benzene are added portionwise 4 parts of 1-iodopropane and the whole is stirred and refluxed for 47 hours. Then the second portion of 4 parts of 1-iodopropane is added and stirring and refluxing is continued for another 20 h.20. The reaction mixture is cooled and filtered. The filtrate is washed with water, dried and evaporated in vacuo. From the oily free base, the hydrochloride salt is prepared in the conventional manner in 1,1'-oxybisethane. The precipitated solid salt is filtered off and dried, yielding 3.5 parts of N-(4-chlorophenyl)-N-(1-propyl-4-piperidinyl)benzeneacetamide hydrochloride; mp. 233.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225606
Source datasetuspto-grants-1980_09
ORD IDord-e2192b2ec0f648c4994e1497b6c9c192
Source noteuspto-grants-1980_09