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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2049601Generated: November 1, 2026

Potassium Iodide → N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide

https://huagongshe.com/reaction/2049601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantBromocyclopentaneHCID 8728—
ReactantSodium CarbonateHCID 10340—
ReactantN-(4-Chlorophenyl)-N-4-piperidinylbenzeneacetamideHCID 162188—
Solvent1-ButanolHCID 263—
ProductN-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamideHCID 20334078—

Reaction Steps

To a stirred and warm (40° C.) mixture of 5 parts of N-(4-chlorophenyl)-N-(4-piperidinyl)benzeneacetamide, 5 parts of sodium carbonate, a few crystals of potassium iodide and 200 parts of n.butanol is added 3.75 parts of bromocyclopentane and the whole is stirred and refluxed for 21h. 30. Then a second portion of 5 parts of bromocyclopentane is added and stirring at reflux temperature is continued for another 30 hours. The reaction mixture is cooled, filtered and the filtrate is evaporated. The oily residue solidifies on triturating in 1,1'-oxybisethane. The solid product is filtered off and crystallized from 1,1'-oxybisethane, yielding 1.1 parts of N-(4-chlorophenyl)-N-(1-cyclopentyl-4-piperidinyl)benzeneacetamide; mp. 139.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04198411
Source datasetuspto-grants-1980_04
ORD IDord-bceaf86e8fc64222a2d6c446cf36f722
Source noteuspto-grants-1980_04