Glyoxal → 6-Bromoquinoxaline

HRID 219127Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 219127
[Br:1][C:2]1[CH:3]=[C:4]([NH2:9])[C:5]([NH2:8])=[CH:6][CH:7]=1.[CH:10](=O)[CH:11]=O>CCO.O>[Br:1][C:2]1[CH:3]=[C:4]2[C:5](=[CH:6][CH:7]=1)[N:8]=[CH:11][CH:10]=[N:9]2

Komponenten

5

Versuchsvorschrift

To a solution of 4-bromobenzene-1,2-diamine (4.0 g, 21 mmol) in 60 mL of EtOH was added 40% glyoxal aldehyde (4.1 ml, 32 mmol) solution in water. The resulting mixture was refluxed for 10 hours. The mixture was concentrated in vacuo and the residue was diluted in 100 mL of EtOAc. The organic solution was washed with 40 mL of satd. NaHCO3 and 40 mL of brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by a silca gel column chromatography (5% EtOAc/hex to EtOAC) to give light yellow solid 6-bromoquinoxaline. MS (ESI, pos. ion) m/z: 208.9 (M+1).

Aufarbeitung

  1. temperatureThe resulting mixture was refluxed for 10 hours
  2. concentrationThe mixture was concentrated in vacuo
  3. additionthe residue was diluted in 100 mL of EtOAc
  4. washThe organic solution was washed with 40 mL of satd
  5. dry with materialNaHCO3 and 40 mL of brine, dried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by a silca gel column chromatography (5% EtOAc/hex to EtOAC)

Quellen und Nachweise

ORD-Eintrag
ord-5ce5b6f5fb3d42748c4b995d5bf0487f
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08198448B2

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