HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413515Generated: October 27, 2026
Potassium Iodide → 5-[4-(diphenylmethyl)-1-piperazinyl]pentyl-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride
https://huagongshe.com/reaction/1413515
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | 1-(5-chloropentyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one | HCID 20506366 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Methyl Isobutyl Ketone | HCID 7909 | — |
| Product | 5-[4-(diphenylmethyl)-1-piperazinyl]pentyl-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride | HCID 86737490 | — |
Reaction Steps
A mixture of 6.95 parts of 1-(5-chloropentyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one, 5.15 parts of 1-(diphenylmethyl)piperazine, 5.30 parts of sodium carbonate, 0.1 parts of potassium iodide and 160 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. The reaction mixture is cooled to room temperature, water is added and the layers are separated. The organic phase is dried filtered and evaporated. The residue is stirred and refluxed for 30 minutes with 12 parts of a hydrochloric acid solution in 40 parts of ethanol. The whole is evaporated and the residue is crystallized from ethanol, yielding 1-{5-[4-(diphenylmethyl)-1-piperazinyl]pentyl-1,3-dihydro-2H-benzimidazol-2-one dihydrochloride.hydrate; mp. 215.3° 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-ebf4414391ec4e0b8bce4f4df845a77b |
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| Source note | uspto-grants-1981_02 |
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