HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741714Generated: October 31, 2026
Diethyl Ether → Benzyl (1-methyl-1H-imidazol-2-yl)carbamate
https://huagongshe.com/reaction/741714
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 1-Methyl-1H-imidazol-2-amine hydrochloride | HCID 10154076 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | Benzyl (1-methyl-1H-imidazol-2-yl)carbamate | HCID 19426850 | — |
Reaction Steps
2-Amino-1-methylimidazole hydrochloride (0.3 g) was dissolved in 1N sodium hydroxide solution (5 ml ). Benzyloxycarbonyl chloride (0.43 g) and ether (2 ml ) were added, and the mixture was stirred for 1 hour. The product was extracted with ethyl acetate, the extract was washed with water and aqueous saturated sodium chloride solution and dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. Diethyl ether-hexane was added to the resulting residue for crystallization, and the crystals were separated by filtration. The crystals of 2-benzyloxycarbonylamino-1-methylimidazole thus obtained was dissolved in chloroform, and 4N hydrochloric acid-ethyl acetate (0.5 ml) was added to form its hydrochloric acid salt. The crude crystals thus obtained were washed with ether to give 2-benzyloxycarbonylamino-1-methylimidazole hydrochloride (0.2 g, Yield: 30% ) as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05552427 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-634ad6d74d3247fdba90e9c2cebf4ff9 |
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| Source note | uspto-grants-1996_09 |
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