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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium HydroxideHCID 14798—
Reactant2,3-Dimethoxyquinoxaline-5-carbaldehydeHCID 15941730—
SolventTrifluoroacetic acidHCID 6422—
Product2,3-Dimethoxy-7-nitroquinoxaline-5-carbaldehydeHCID 23297985—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080743
Source datasetuspto-grants-2000_06
ORD IDord-2ccda73892ad4de9b059899ee0e21e65
Source noteuspto-grants-2000_06