HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413513Generated: October 30, 2026
Potassium Iodide → Diphenylmethyl piperazinylbenzimidazole
https://huagongshe.com/reaction/1413513
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | 1-(3-Chloropropyl)-1H-benzimidazole | HCID 13105517 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | Diphenylmethyl piperazinylbenzimidazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04250176 |
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| Source dataset | uspto-grants-1981_02 |
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| ORD ID | ord-8c3be44239a3455caa5d521672963185 |
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| Source note | uspto-grants-1981_02 |
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