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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729820Generated: November 3, 2026

Potassium Iodide → 5-chloro-1,3-dihydro-1-[1-(4,4-diphenylbutyl)-4-piperidinyl]-2-H-benzimidazol-2-one

https://huagongshe.com/reaction/1729820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant1,1'-(4-Chlorobutylidene)bisbenzeneHCID 76821—
Reactant5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-oneHCID 104607—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product5-chloro-1,3-dihydro-1-[1-(4,4-diphenylbutyl)-4-piperidinyl]-2-H-benzimidazol-2-oneHCID 21500248—

Reaction Steps

A mixture of 7.35 parts of 1-chloro-4,4-diphenylbutane, 6.3 parts of 5-chloro-1-(4-piperidyl)-2-benzimidazolinone, 6.35 parts of sodium carbonate, 0.1 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed for 48 hours with water-separator. The reaction mixture is cooled to room temperature and water is added. The organic layer is separated, dried, filtered and evaporated. The residue is crystallized twice; first from 2-propanol and then from 4-methyl-2-pentanone, yielding 5-chloro-1,3-dihydro-1-[1-(4,4-diphenylbutyl)-4-piperidinyl]-2-H-benzimidazol-2-one; mp. 164.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989707
Source datasetuspto-grants-1976_11
ORD IDord-9915b96491b245c1b203fdebb92d327a
Source noteuspto-grants-1976_11