Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylglyoxal | HCID 880 | — |
| Reactant | 4-Nitro-1,2-phenylenediamine | HCID 5111791 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 824610 | HCID 824610 | 60% |
Reaction Steps
To a suspension of 4-nitro-1,2-phenylenediamine (10.0 g) in water (150 mL) was added dropwise a 40% aqueous solution of pyruvic aldehyde (11.76 g) at room temperature. The reaction solution was stirred at 80° C. for 4 hours, and cooled to room temperature. Water (200 mL) was added to the mixture, and the mixture was extracted with chloroform (150 mL×3). The organic layers were combined, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residual solid was recrystallized from ethanol, collected by filtration, and dried to give 2-methyl-6-nitroquinoxaline (7.38 g, 60%) as red solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06759429B2 |
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| Source dataset | uspto-grants-2004_07 |
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| ORD ID | ord-44b6a759491a4225b53997de669fd402 |
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| Source note | uspto-grants-2004_07 |
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