Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | HCID 387928 | HCID 387928 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Solvent | Ethyl acetate hexane | HCID 21226206 | — |
| Product | HCID 18369162 | HCID 18369162 | 41% |
Reaction Steps
To a solution of ethyl 3,4-dihydro-3-oxo-6-trifluoromethylquinoxaline-2-carboxylate (500 mg, 1.75 mmol) in concentrated sulfuric acid (5 ml) was added potassium nitrate (354 mg, 3.50 mmol) at 40° C., and the mixture was stirred for 3 hours at the same temperature. The reaction mixture was poured into ice water (100 ml), which was extracted with ethyl acetate. After dried over anhydrous sodium sulfate, solvent was distilled off. Silver oxide (I)(811 mg, 3.50 mmol) was added to the residue obtained which was suspended into toluene (10 ml). Then, iodoethane (280 μl, 3.50 mmol) was added dropwise at 100° C. and the mixture was refluxed for 2 hours. After cooling, the insolubles were filtered off using celite and the solvent was distilled off. The residue obtained was submitted to silica gel column chromatography [hexane-ethyl acetate=8:1] to obtain 255 mg of the title compound as yellowish brown oily product. Yield 41%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06348461B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-394f1e170aba4861b7e4218678eeb83c |
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| Source note | uspto-grants-2002_02 |
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