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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050303Generated: November 2, 2026

Potassium Iodide → Diphenylmethyl piperazinylbenzimidazole

https://huagongshe.com/reaction/2050303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
ReactantBenzhydrylpiperazineHCID 70048—
Reactant1-(3-Chloropropyl)-1H-benzimidazoleHCID 13105517—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
ProductDiphenylmethyl piperazinylbenzimidazoleHCID 13105518—

Reaction Steps

A mixture of 4.5 parts of 1-(3-chloropropyl)-1H-benzimidazole, 5.1 parts of 1-(diphenylmethyl)piperazine, 3.7 parts of sodium carbonate, 0.1 parts of potassium iodide and 80 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of 4-methyl-2-pentanone and 2,2'-oxybispropane, yielding 1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1H-benzimidazole; mp. 132.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200641
Source datasetuspto-grants-1980_04
ORD IDord-e1cbffa1872444ca8c54d1ee4592efc7
Source noteuspto-grants-1980_04