HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965174Generated: October 30, 2026
Hydrochloric Acid → HCID 54712961, compound
https://huagongshe.com/reaction/965174
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(1H-Imidazol-1-yl)ethanone | HCID 17174 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19076040 | HCID 19076040 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 54712961 | HCID 54712961 | — |
Reaction Steps
2-Cyano-N-(3-methyl-4-nitrophenyl)acetamide (0.61 g; 2.8 mmol) is dissolved in tetrahydrofuran (30 ml) and sodium hydride (80% strength dispersion in oil; 0.21 g; 7 mmol) is added. The mixture is stirred at 25° C. for 15 minutes and 1-acetylimidazole (0.46 g; 4.2 mmol) is added dropwise over the course of 5 minutes and the mixture is stirred for a further 15 minutes. 2 ml of glacial acetic acid are added and the mixture is stirred at 25° C. for 1 hour and then poured into ice-cold water (100 ml). The pH of the solution is then adjusted to 1 using concentrated hydrochloric acid, and the precipitate is filtered, washed with water and brought to dryness under reduced pressure. N-(3-Methyl-4-nitrophenyl)-2-cyano-3-hydroxycrotonamide is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773470 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-78fcc7d80ae14e8fb17b1fbee8396d66 |
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| Source note | uspto-grants-1998_06 |
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