HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354922Generated: October 25, 2026
1,6-Dichlorohexane → 1-(6-chlorohexyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one
https://huagongshe.com/reaction/354922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,6-Dichlorohexane | HCID 16551 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1,3-Dihydro-1-(1-methylvinyl)-2H-benzimidazol-2-one | HCID 100278 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(6-chlorohexyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one | HCID 20506339 | — |
Reaction Steps
To a stirred mixture of 3.2 parts of a sodium hydride dispersion 70% in 9 parts of N,N-dimethylformamide is added dropwise (slowly), during a 2 hours-period, a mixture of 17.4 parts of 1,3-dihydro-1-(1-methylethenyl)-2H-benzimidazol-2-one, 77.5 parts of 1,6-dichlorohexane and 36 parts of N,N-dimethylformamide. Upon completion, stirring is continued overnight at room temperature. The reaction mixture is filtered over hyflo and the N,N-dimethylformamide is evaporated in vacuo. The excess of 1,6-dichlorohexane is distilled off in an oil-bath with water-jet. The residue is dissolved in methylbenzene and the solution is stirred with activated charcoal. The latter is filtered off over hyflo and the filtrate is evaporated, yielding 1-(6-chlorohexyl)-1,3-dihydro-3-(1-methylethenyl)-2H-benzimidazol-2-one as an oily residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04377578 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-9de3e9885712420993bb5ecef6f7d113 |
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| Source note | uspto-grants-1983_03 |
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