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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54406Generated: October 30, 2026

Potassium Nitrate → 6-Bromo-7-chloro-5-nitro-1,4-dihydro-2,3-quinoxalinedione

https://huagongshe.com/reaction/54406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
Reactant6-Bromo-7-chloro-5-nitroquinoxaline-2(1H)-oneHCID 21189985—
SolventSulfuric AcidHCID 1118—
Product6-Bromo-7-chloro-5-nitro-1,4-dihydro-2,3-quinoxalinedioneHCID 1040375150%

Reaction Steps

To a stirred solution of 6-bromo-7-chloro-5-nitroquinoxaline-2(1H)-one (0.025 g, 0.082 mmol) in conc. H2SO4 (0.5 mL) was added KNO3 (0.011 g, 0.11 mmol) and the resulting dark red solution was stirred at r.t. for 65 h. The solution was then cooled in an ice-bath and diluted with ice to a total volume of 5.0 mL. The precipitated solid was filtered, washed with water (2.0 mL) and dried under vacuum to give 0.019 g (72%) of crude product. It was purified as follows. Crude product (0.016 g) was taken up in 1N NaOH (1.1 mL). The mixture was centrifuged and the supernatant liquid was acidified with conc. HCl to pH~2. The precipitated solid was filtered, washed with water (1.0 mL) and dried under vacuum to furnish 0.010 g (50%) of pure title compound as a cream colored powder; m.p. 338°-343° C. (decomposed); 1H NMR (DMSO-d6): 7.35 1 (s, 1H), 12.25 1 (s overlapped by a br s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622952
Source datasetuspto-grants-1997_04
ORD IDord-74d407f01a4b4db4ab2e20a303453c75
Source noteuspto-grants-1997_04