HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53729Generated: October 26, 2026
Potassium Nitrate → 6-Fluoro-7-nitro-1,4-dihydroquinoxaline-2,3-dione
https://huagongshe.com/reaction/53729
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | 6-Fluoro-1,4-dihydro-2,3-quinoxalinedione | HCID 601953 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | 6-Fluoro-7-nitro-1,4-dihydroquinoxaline-2,3-dione | HCID 9991230 | 70% |
Reaction Steps
The title compound was prepared using an adaptation of the method of Cheeseman (Cheeseman, G. W. H., J. Chem. Soc. 1171 (1962)). 6-Fluoro-1,4-dihydroquinoxaline-2,3-dione (200 mg, 1.10 mmol) was dissolved in 3 mL of concentrated H2SO4 and the blue green solution was cooled to 0° C. with stirring. To this was added in small portions KNO3 (110 mg, 1.10 mmol). The reaction was allowed to stir 1 h at 0° C. and then was allowed to come to room temperature and stir overnight. The brown-orange reaction mixture was then poured into 10 mL ice/H2O. The product was isolated by vacuum filtration as brown crystals which were rinsed with a small amount of cold H2O and air dried. The crystals were further dried under vacuum (0.1 torr, 25° C.) to yield 173.4 mg (70.0% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05620979 |
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| Source dataset | uspto-grants-1997_04 |
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| ORD ID | ord-3cda9a04796b4592847a826a3c2e6426 |
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| Source note | uspto-grants-1997_04 |
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