HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276068Generated: October 27, 2026
Potassium Iodide → 1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-2-methylbenzimidazole
https://huagongshe.com/reaction/276068
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | ethyl 2-methyl-1H-benzimidazole-4-carboxylate | HCID 18680979 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(2,4-Dichlorobenzyl)-4-ethoxycarbonyl-2-methylbenzimidazole | HCID 18681089 | 25.5% |
Reaction Steps
A mixture of 1.61 g of 4-ethoxycarbonyl-2-methylbenzimidazole, 3.08 g of 2,4-dichlorobenzyl chloride, 1.51 g of potassium iodide, 1.05 g of potassium carbonate and 4 ml of N,N-dimethylformamide was stirred at 80° C. for 16 hours. The reaction mixture was extracted with chloroform and with water. The chloroform layer was washed with water, dried, and concentrated. The residue was purified through silica-gel column chromatography (eluent: a mixture of hexane and ethyl acetate at a ratio of 2:8) to give 0.730 g of 1-(2,4-dichlorobenzyl)-4-ethoxycarbonyl-2-methylbenzimidazole (297).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06352985B1 |
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| Source dataset | uspto-grants-2002_03 |
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| ORD ID | ord-03f3532da7084458901a2f2a057bfb80 |
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| Source note | uspto-grants-2002_03 |
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