Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2,3-Dihydroxy-6,7-dichloroquinoxaline | HCID 1845 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Phosphorus pentabromide | HCID 62678 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 15418643 | HCID 15418643 | 94% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548499B1 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-e43be34d665b4747a378daf1c82b2823 |
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| Source note | uspto-grants-2003_04 |
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