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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833657Generated: October 27, 2026

Potassium Iodide → 6-chloro-1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/1833657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant4-(4-Chlorophenyl)-4-hydroxypiperidineHCID 38282—
Reactant6-chloro-1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-oneHCID 20385587—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product6-chloro-1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-oneHCID 20385624—

Reaction Steps

A mixture of 5.6 parts of 6-chloro-1-(3-chloro-propyl)-1,3-dihydro-2H-benzimidazol-2-one, 4.2 parts of 4-(4-chloropheny)-4-piperidinol, 6.4 parts of sodium carbonate, 0.2 parts of potassium iodide and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. After cooling, water is added and the layers are separated. The 4-methyl-2-pentanone-phase is dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The solid residue is crystallized from 4-methyl-2-pentanone, yielding 3.5 parts of 6-chloro-1-{3-[4-(4-chlorophenyl)-4-hydroxy-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 180.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066772
Source datasetuspto-grants-1978_01
ORD IDord-6dbd63e37a3c4472a377763a560b59c5
Source noteuspto-grants-1978_01