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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413514Generated: November 3, 2026

Potassium Iodide → 1-[3-{4-[(2-chlorophenyl)phenylmethyl]-1-piperazinyl}propyl]1H-benzimidazole trihydrochloride dihydrate

https://huagongshe.com/reaction/1413514

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant1-(3-Chloropropyl)-1H-benzimidazoleHCID 13105517—
Reactant1-[(2-Chlorophenyl)phenylmethyl]piperazine acetateHCID 70534570—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product1-[3-{4-[(2-chlorophenyl)phenylmethyl]-1-piperazinyl}propyl]1H-benzimidazole trihydrochloride dihydrateHCID 70535024—

Reaction Steps

A mixture of 4.9 parts of 1-(3-chloropropyl)-1H-benzimidazole, 7 parts of 1-[(2-chlorophenyl)phenylmethyl]piperazine acetate, 10.6 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 20 hours with water-separator. The reaction mixture is cooled, water is added and the layers are separated. The organic phase is dried, filtered and evaporated. The residue is converted into the hydrochloride salt in 2-propanol and 2,2'-oxybispropane. The salt is filtered off and crystallized from 2-propanol, yielding 1-[3-{4-[(2-chlorophenyl)phenylmethyl]-1-piperazinyl}propyl]1H-benzimidazole trihydrochloride dihydrate; mp. 182.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04250176
Source datasetuspto-grants-1981_02
ORD IDord-8e0da58f29f8493889059b33a505c49e
Source noteuspto-grants-1981_02