HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2164805Generated: November 1, 2026
Hydrochloric Acid → 2-(2-Nitrobenzyl)-imidazole
https://huagongshe.com/reaction/2164805
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | Ethyl 2-(2-nitrophenyl)acetimidate hydrochloride | HCID 13344902 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-(2-Nitrobenzyl)-imidazole | HCID 11206478 | — |
Reaction Steps
Ethanol (2,200 ml) and5,156 g (8.81 moles) of ethyl 2-(2-nitrophenyl)acetimidate hydrochloride are charged into a 22 liter flask. The suspension is stirred under nitrogen at room temperature and 1022.9 g (9.73 moles) of aminoacetaldehyde dimethylacetal are added all at once. The mixture is stirred for 1 hour and 1,693 ml of 12N hydrochloric acid are added all at once to cause a gentle exotherm (to 40°). Heat is then applied and the temperature is maintained at 70°-80° for 30 minutes. The solution is cooled to 20° (ice-water bath) and diluted with 2,700 ml of 10N sodium hydroxide solution to precipitate the product. The suspension is stirred at 10° for 1 hour under nitrogen atmosphere, the solid collected by filtration and washed with 3×2,000 ml of water to give 2-(2-nitrobenzyl)imidazole, m.p. 155°-7°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04507311 |
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| Source dataset | uspto-grants-1985_03 |
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| ORD ID | ord-2fd0c2ea782b4bcaa761b7cff97eddb4 |
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| Source note | uspto-grants-1985_03 |
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