HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741713Generated: October 29, 2026
Ethyl chloroformate → Ethyl (1-methyl-1H-imidazol-2-yl)carbamate
https://huagongshe.com/reaction/741713
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 1-Methyl-1H-imidazol-2-amine hydrochloride | HCID 10154076 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Ethyl (1-methyl-1H-imidazol-2-yl)carbamate | HCID 15837347 | — |
Reaction Steps
Ethyl chlorocarbonate (0.6 g) was added to a solution of 2-amino-1-methylimidazole hydrochloride (0.3 g) in pyridine (5 ml), and the mixture was stirred under heating at 100° C. for 2 hours. The solvent was evaporated under reduced pressure, the residue was dissolved in water, and sodium carbonate was added until the solution became alkaline. The solvent was evaporated under reduced pressure, and then the residue was purified by column chromatography on silica gel (eluent: chloroform) to give 2-ethoxycarbonylamino-1-methylimidazole. This compound was dissolved in dichloromethane, and 4N hydrochloric acid-ethyl acetate (2 ml) was added to form its hydrochloric acid salt. The resulting crude crystals were washed with ether to give 2-ethoxycarbonylamino-1-methylimidazole hydrochloride (0.29 g, Yield: 56%) as colorless prisms.
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-9d6234d79398474d947f533661f03d54 |
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| Source note | uspto-grants-1996_09 |
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