HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495230Generated: October 26, 2026
Benzyl Chloride → 1-Benzyl-4-methyl-1H-benzimidazole
https://huagongshe.com/reaction/495230
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methylbenzimidazole | HCID 1519341 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyl-4-methyl-1H-benzimidazole | HCID 14933024 | — |
Reaction Steps
To a flask were added 1.0 g 4-methyl-1H-benzimidazole, 1.6 g potassium carbonate, 25 ml N,N-dimethylformamide and the mixture was stirred under nitrogen. 1.4 g Benzyl chloride were added and the mixture was heated to 60 C for 16 hours. Another 0.4 g of benzyl chloride were added and the reaction was heated to 70 C for 24 hours. The reaction was cooled to 50 C and quenched with 50 ml water and extracted with ethyl acetate. After washing with water, the solvent was removed and the product was purified by column chromatography using a gradient from 40% ethyl acetate in hexane to 75% ethyl acetate in hexane. Following removal of the solvent, the partially crystallized product was dissolved in 20 ml acetonitrile and treated with 0.1 g activated carbon. After refluxing for 20 minutes, the mixture was filtered through celite and the solvent was removed leaving a yellow oil which crystallized on standing, 1.0 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538931B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-218b782235a04ad585e99327bd7560fa |
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| Source note | uspto-grants-2009_05 |
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