HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 988068Generated: October 30, 2026
1-Methylimidazole → ethyl 1-methyl-1H-imidazole-2-carboxylate
https://huagongshe.com/reaction/988068
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | ethyl 1-methyl-1H-imidazole-2-carboxylate | HCID 4261883 | 82% |
Reaction Steps
N-methylimidazole (320 g, 3.9 mol) was combined with 2 L acetonitrile and 1 L triethylamine in a 12 L flask equipped with a mechanical stirrer and the solution cooled to −20° C. Ethyl chloroformate (1000 g, 9.2 mol) was added with stirring, keeping the temperature between −20° C. and −25° C. The reaction was allowed to lowly warm to room temperature and stir for 36 h. Precipitated triethylamine hydrochloride was removed by filtration and the solution concentrated in vacuo at 65° C. The resulting oil was purified by distillation under reduced pressure (2 torr, 102° C.) to provide a white solid (360 g, 82% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06635417B1 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-0af0c12a71574c4ab2e6ec57258eefa6 |
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| Source note | uspto-grants-2003_10 |
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