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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26759Generated: October 25, 2026

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

https://huagongshe.com/reaction/26759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylethylamineHCID 11723—
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-dimethylethanamine 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 20h.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. 235.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151286
Source datasetuspto-grants-1979_04
ORD IDord-808cb0a0266748a798ce898cc0ed978c
Source noteuspto-grants-1979_04