HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 709929Generated: November 1, 2026
Potassium Carbonate → ethyl 1-amino-1H-imidazole-2-carboxylate
https://huagongshe.com/reaction/709929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | ethyl 1H-imidazole-2-carboxylate | HCID 549404 | — |
| Solvent | Water | HCID 962 | — |
| Product | ethyl 1-amino-1H-imidazole-2-carboxylate | HCID 58332105 | — |
Reaction Steps
To a stirred solution of hydroxylamine-o-sulfonic acid (26.64 g, 235.8 mmol, 3.0 eq) in H2O (17 mL) at 0° C., ethyl 1H-imidazole-2-carboxylate (C-3) (11.0 g, 78.6 mmol, 1.0 eq) is added and the resulting mixture is stirred at 90° C. for 30 min. The mixture is cooled to RT and K2CO3 (3.6 g, 26.2 mmol, 1.0 eq) is added in portions. The resulting mixture is stirred at RT overnight, filtered and rinsed with H2O (10 mL×3). The filtrate is extracted with ethyl acetate (50 mL×5). The combined organic layer is washed with brine, dried over Na2SO4 and filtered. The filtrate is evaporated in vacuo and the residue is purified by flash column chromatography on silica gel (1% MeOH-DCM) to afford the product, ethyl 1-amino-1H-imidazole-2-carboxylate (C-4) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181221B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-c5409a8201f34b709f1ec0300a11ff81 |
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| Source note | uspto-grants-2015_11 |
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