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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant1-Methyl-1H-imidazol-2-amine hydrochlorideHCID 10154076—
SolventPyridineHCID 1049—
ProductEthyl (1-methyl-1H-imidazol-2-yl)carbamateHCID 15837347—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552427
Source datasetuspto-grants-1996_09
ORD IDord-9d6234d79398474d947f533661f03d54
Source noteuspto-grants-1996_09