HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707662Generated: November 1, 2026
Hydrochloric Acid → 1H-Imidazole, 2-(2-benzofuranyl)-1-methyl-, monohydrochloride
https://huagongshe.com/reaction/1707662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1H-Imidazole, 2-(2-benzofuranyl)-, monohydrochloride | HCID 3073595 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Diethyl ether ethanol | HCID 21585056 | — |
| Product | 1H-Imidazole, 2-(2-benzofuranyl)-1-methyl-, monohydrochloride | HCID 3073597 | — |
Reaction Steps
To a solution of the free base (7.0 g) generated from 2-(benzofuran-2-yl)imidazole hydrochloride in DMF (50 ml) at 0° C. was added sodium hydride (1.4 g) 80% in mineral oil in three equal portions. After 30 minutes at room temperature, methyl iodide (2.5 ml) was added dropwise over 15 minutes at 0° C. The mixture was then stirred for 30 minutes at room temperature, poured into water and extracted with ethyl acetate. The organic layer was washed with water and the product was extracted with hydrochloric acid (1M). The aqueous layer was basified with sodium hydroxide and the free base was extracted with ethyl acetate, washed with saturated brine and dried. Evaporation of the solvent gave a solid residue which was dissolved in diethyl ether/ethanol. Ethereal HCl was added to solution and the precipitated salt was collected by filtration (8.1 g, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354769 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-19ec5445c00f4e16a0ee0c4a8f5a4475 |
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| Source note | uspto-grants-1994_10 |
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