HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707661Generated: November 1, 2026
Hydrochloric Acid → 1H-Imidazole, 2-(2-benzofuranyl)-, monohydrochloride
https://huagongshe.com/reaction/1707661
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | HCID 18962029 | HCID 18962029 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl ether ethanol | HCID 21585056 | — |
| Product | 1H-Imidazole, 2-(2-benzofuranyl)-, monohydrochloride | HCID 3073595 | — |
Reaction Steps
A solution of aminoacetaldehyde dimethylacetal (7.3 g) and methyl benzofuran-2carboximidate hydrochloride (13.4 g) in methanol (135 ml) was stirred at 60° C. for 16 hours. The mixture was then evaporated to dryness. Hydrochloric acid (750 ml, 2M) was added and the resulting mixture was stirred at 60° C. for 16 hours. After cooling, the solution was washed with dichloromethane. The aqueous layer was basified with sodium hydroxide and the free base was extracted with ethyl acetate. The organic layer was 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 (12.5 g, 90%).
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-b9b2d16cdf8842dda987273904239159 |
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| Source note | uspto-grants-1994_10 |
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