Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53739Generated: October 28, 2026

Potassium Nitrate → Acea-1031

https://huagongshe.com/reaction/53739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
Reactant6,7-Dibromo-1,4-dihydroquinoxaline-2,3-dioneHCID 15021835—
SolventSulfuric AcidHCID 1118—
ProductAcea-1031HCID 979920176%

Reaction Conditions

Temperature0 °C

Reaction Steps

The procedure of Cheeseman, G. W. H., J. Chem Soc. 1170 (1962) was adapted. To a stirred suspension of 6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione (576 mg, 1.8 mMol) in concentrated H2SO4 (6 mL) at 0° C. for 30 min. was added KNO3 (220 mg, 2.18 mMol, Baker) in one portion. The mixture was stirred at 0° C. for 3 h then at room temperature for one day. The color of mixture was changed from red to yellow brown. Then it was poured into ice (60 g) resulting in the separation of a bright yellow precipitate, which was collected by filtration and washed with distilled water (2×2 mL) followed by ethanol (2×1 mL) to get 498 mg of crude 5-nitro-6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione (76%, contains minor impurities by NMR). Crystallization from DMSO/H2O gave pure 5-nitro-6,7-dibromo-1,4-dihydro-2,3-quinoxalinedione as bright yellow microcrystals; mp: 352°-354° C. (dec.). IR (KBr, cm-1): 3387; 3256; 1756; 1700; 1537. NMR (1H, DMSO-d6): δ 7.475 (s, 1H); 12.217 (s, 1H); 12.265 (s, 1H). HRMS: calcd for C8H3N3O4Br2 (M+) m/z: 362.8489; found: 362.8509.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620979
Source datasetuspto-grants-1997_04
ORD IDord-8d2cbc858dba4a89aee30ffbe9f96200
Source noteuspto-grants-1997_04