HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916376Generated: November 1, 2026
Ethyl chloroacetate → ethyl (2-formyl-1H-imidazol-1-yl)acetate
https://huagongshe.com/reaction/1916376
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl (2-formyl-1H-imidazol-1-yl)acetate | HCID 62222097 | — |
Reaction Steps
To 1H-imidazole-2-carboaldehyde (2.0 g), N-methylpyrrolidone (25 mL) was added, followed by dissolution with heating. To the resultant solution, ethyl chloroacetate (11.1 mL) and potassium carbonate (2.9 g) were added. The reaction solution was stirred at room temperature for 14 hours. To the reaction solution, water (30 mL) was added. The aqueous layer was extracted twice with ethyl acetate. The organic layers were combined, washed with saturated saline and then dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was removed by filtration and the solvent was concentrated under reduced pressure. The residue was purified by silica gel chromatography (dichloromethane) to obtain the title compound having the following physical properties (1.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08618122B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-0565e269818249d3a4ce5913ed66a94e |
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| Source note | uspto-grants-2013_12 |
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