HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422252Generated: November 2, 2026
Nitric Acid → 2,3-Dimethoxy-7-nitroquinoxaline-5-carbaldehyde
https://huagongshe.com/reaction/1422252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,3-Dimethoxyquinoxaline-5-carbaldehyde | HCID 15941730 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 2,3-Dimethoxy-7-nitroquinoxaline-5-carbaldehyde | HCID 23297985 | — |
Reaction Steps
44 ml of 100% nitric acid, 44 ml of 97% sulfuric acid and 44 ml of trifluoroacetic anhydride are added in succession to a solution, cooled to 0° C., of 22 g (100.8 mmol) of 2,3-dimethoxy-quinoxaline-5-carbaldehyde in 88 ml of trifluoroacetic acid. The mixture is maintained at 0° C. for 2 hours and is then carefully poured onto a mixture of 4N NaOH and ice. The temperature should not exceed 20° C. The mixture is extracted with ethyl acetate. The organic phase is washed with an aqueous 1 N NaOH solution, water and brine and dried over sodium sulfate. Crystallization of the crude product yields the title compound in the form of light-yellow crystals. M.p.: 147-149° C.; TLC (EtOAc/hexane 1:3): Rf =0.25.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06080743 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-2ccda73892ad4de9b059899ee0e21e65 |
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| Source note | uspto-grants-2000_06 |
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