Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54333Generated: October 25, 2026

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

https://huagongshe.com/reaction/54333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium NitrateHCID 24434—
Reactant5-Bromo-7-fluoro-1,4-dihydroquinoxaline-2,3-dioneHCID 21190039—
SolventSulfuric AcidHCID 1118—
Product5-Bromo-6-nitro-7-fluoro-1,4-dihydro-2,3-quinoxalinedioneHCID 1995862190%

Reaction Conditions

Temperature0 °C

Reaction Steps

The method of Cheeseman, supra. was adapted. 5-Bromo-7-fluoro-1,4-dihydroquinoxaline-2,3-dione (77 mg, 0.30 mMol) was dissolved in concentrated H2SO4 (1 mL) at 0° C. for 30 min, and KNO3 (35 mg, 0.346 mMol, Baker) was added to this solution. The mixture was stirred at 0° C. for 3 h and then at room temperature for 30 h. The mixture was poured into ice water (10 g) and the precipitate was collected by filtration. The precipitate was dissolved in 1N NaOH (10 mL), then was acidified to pH=2 with 4N HCl to give cream precipitate, which was collected by filtration, and was dried in the air at 50° C. for 4 h affording pure (by NMR) 5-bromo-6-nitro-7-fluoro-1,4-dihydro-2,3-quinoxalinedione (81 mg, 90%), as a white amorphous solid; mp: 320°-25° C. (dec. from 290° C.). IR (KBr, cm-1): 3416, 3071, 2952, 1721, 1609, 1546. NMR (1H, DMSO-d6): δ7.146 (d, J=10.2 Hz, 1H), 11.432 (s, 1H), 12.340 (s, 1H). HRMS: calcd. for C8H3N3O4BrF (M+) m/z: 302.9290, found: 302.9290.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622952
Source datasetuspto-grants-1997_04
ORD IDord-b18cf801faaa417a97074c34eb28c70a
Source noteuspto-grants-1997_04