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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704509Generated: October 26, 2026

Potassium Iodide → 8-[3-(1H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one

https://huagongshe.com/reaction/1704509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantSodium CarbonateHCID 10340—
Reactant1-Phenyl-1,3,8-triazaspiro(4.5)decan-4-oneHCID 70556—
Reactant1-(3-Chloropropyl)-1H-benzimidazoleHCID 13105517—
SolventWaterHCID 962—
SolventMethyl Isobutyl KetoneHCID 7909—
Product8-[3-(1H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-oneHCID 2038563925%

Reaction Steps

A mixture of 6 parts of 1-(3-chloropropyl)-1H-benzimidazole, 4.6 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one, 10 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 (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 2 parts (25%) of 8-[3-(1H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one; mp. 191° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126687
Source datasetuspto-grants-1978_11
ORD IDord-96b49f3f0a504404b35f5327b69be3ad
Source noteuspto-grants-1978_11