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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266134Generated: November 4, 2026

Hydrogen Bromide → HCID 15418643, compound

https://huagongshe.com/reaction/1266134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2,3-Dihydroxy-6,7-dichloroquinoxalineHCID 1845—
ReactantAmmonium HydroxideHCID 14923—
ReactantPhosphorus pentabromideHCID 62678—
SolventSodium HydroxideHCID 14798—
ProductHCID 15418643HCID 1541864394%

Reaction Conditions

Temperature155 °C

Reaction Steps

6,7-Dichloro-1,4-dihydro-quinoxaline-2,3-dione (5.39 g, 23.3 mmol) and phosphorus pentabromide (20.1 g, 46.7 mmol) were charged in a 100 mL round-bottom flask equipped with a condenser with an outlet half immerged in 10% NaOH aqueous solution (to absorb HBr generated during the reaction). The reaction was heated at 155° C. using an oil-bath for 2 hours when the formation of HBr ceased. The reaction content was poured into ice-water (100 mL) and basified with NH4OH. After filtration, the solid was dried and recrystallized using EtOH to give the desired product as a white solid (7.84 g, 94% yield): mp 169-70° C.; Rf=0.50, CH2Cl2; IR (KBr, cm−1) 3088, 1539, 1451, 1240, 1128, 964, 997; 1H NMR (CDCl3) δ 8.13 (s, 2H); 13C NMR (CDCl3) δ 142.4, 139.7, 136.3; MS (ACPI), m/z 338.4 (MH+); Anal. Calcd for C8H2N2Cl2Br2: C, 26.93; H, 0.56; N, 7.85. Found: C, 26.93; H, 0.56; N, 7.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548499B1
Source datasetuspto-grants-2003_04
ORD IDord-e43be34d665b4747a378daf1c82b2823
Source noteuspto-grants-2003_04