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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616992Generated: October 29, 2026

Potassium Iodide → 2H-Benzimidazol-2-one, 1,3-dihydro-1-(1-(4,4-bis(4-fluorophenyl)cyclohexyl)-4-piperidinyl)-5-chloro-

https://huagongshe.com/reaction/616992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 104607—
ReactantHCID 20366914HCID 20366914—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product2H-Benzimidazol-2-one, 1,3-dihydro-1-(1-(4,4-bis(4-fluorophenyl)cyclohexyl)-4-piperidinyl)-5-chloro-HCID 3045900—

Reaction Steps

A mixture of 11 g of 4,4-bis(p-fluorophenyl)cyclohexyl tosylate, 6 g of 1-(4-piperidyl)-5-chloro-2-benzimidazolinone, 3.5 g of potassium carbonate, 4.1 g of potassium iodide and 80 ml of dimethylformamide is stirred at 70°-80° C for 64 hours. The reaction mixture is poured into water, ether is added to the separated semi-solid, and the whole is stirred for 30 minutes. The substance insoluble in water and ether is collected by filtration, washed with ether and dried. The obtained crystals are dissolved in a mixture of chloroform and methanol (9:1), and the solution is concentrated to some degree and cooled. The precipitated crystals are collected by filtration and purified in the same manner to give 1-[1-(4,4-bis(p-fluorophenyl)cyclohexyl)-4-piperidyl]-5-chloro-2-benzimidazolinone as white crystals, melting at 279°-284° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04076821
Source datasetuspto-grants-1978_02
ORD IDord-30367c1dca2c45798308895eb59e9ad0
Source noteuspto-grants-1978_02