HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704596Generated: October 30, 2026
Methyl Isobutyl Ketone → HCID 20385629, compound
https://huagongshe.com/reaction/1704596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Isobutyl Ketone | HCID 7909 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one | HCID 104607 | — |
| Reactant | HCID 3732348 | HCID 3732348 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20385629 | HCID 20385629 | 25% |
Reaction Steps
A mixture of 5 parts of 5-chloro-1,3-dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one, 3.7 parts of sodium carbonate and 200 parts of 4-methyl-2-pentanone is stirred and refluxed with water-separator. Then there are added 4.8 parts of 1-(3-bromopropyl)-1H-benzotriazole and stirring is continued overnight at reflux temperature. The reaction mixture is cooled, water is added and the undissolved product is filtered off and set aside. The organic phase is separated from the filtrate, dried, filtered and evaporated. The residue is combined with the undissolved product (see above) and 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 4-methyl-2-pentanone, yielding 2 parts (25%) of 1-{1-[3-(1H-benzotriazol-1-yl)propyl]-4-piperidinyl}-5-chloro-1,3-dihydro-2H-benzimidazol-2-one; mp. 203.4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04126688 |
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| Source dataset | uspto-grants-1978_11 |
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| ORD ID | ord-371f76343da24ac295070c9c9c21c727 |
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| Source note | uspto-grants-1978_11 |
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