HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1413529Generated: November 3, 2026
Methyl Isobutyl Ketone → 1-{3-[4-(diphenylmethoxy)-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one
https://huagongshe.com/reaction/1413529
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one | HCID 1810419 | — |
| Reactant | 4-(Diphenylmethoxy)piperidinium chloride | HCID 44153518 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-{3-[4-(diphenylmethoxy)-1-piperidinyl]propyl}-1,3-dihydro-2H-benzimidazol-2-one | HCID 13105611 | — |
Reaction Steps
A mixture of 4.8 parts of 1-(3-chloropropyl)-1,3-dihydro-2H-benzimidazol-2-one, 6.1 parts of 4-(diphenylmethoxy)piperidine hydrochloride, 7.5 parts of sodium carbonate and 200 parts of 4-methyl-2-pentanone is stirred and refluxed overnight with water-separator. The reaction mixture is cooled and water is added. The layers are separated and 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 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 4-methyl-2-pentanone, yielding 1-{3-[4-(diphenylmethoxy)-1-piperidinyl]-propyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 149.2° 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-adeb3c4395024584a9dc4584afa1c813 |
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| Source note | uspto-grants-1981_02 |
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