1,1'-Oxalyldiimidazole → 5-Hydroxy-1,4-dihydroquinoxaline-2,3-dione

HRID 2191388Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2191388
[NH2:1][C:2]1[C:7]([NH2:8])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:9].[C:10](N1C=CN=C1)(=[O:18])[C:11](N1C=CN=C1)=[O:12]>O1CCCC1>[OH:9][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:2]=1[NH:1][C:10](=[O:18])[C:11](=[O:12])[NH:8]2

Komponenten

4

Versuchsvorschrift

A solution of 2,3-diaminophenol (50 g). and 1,1′-oxalyldiimidazole (92 g) and tetrahydrofurane (1.2 L) is refluxed 30 minutes. The solvent is removed under reduced pressure and the remaining solid taken into ethyl acetate. The organic phase is washed with 1M aqueous hydrochloric solution, dried over sodium sulphate and concentrated under vacuum. The crude solid obtained is recrystallised from dimethylformamide; yield: 14.8 g; MS: 177.1 (M−1);

Aufarbeitung

  1. customThe solvent is removed under reduced pressure
  2. washThe organic phase is washed with 1M aqueous hydrochloric solution
  3. dry with materialdried over sodium sulphate
  4. concentrationconcentrated under vacuum
  5. customThe crude solid obtained
  6. customis recrystallised from dimethylformamide

Quellen und Nachweise

ORD-Eintrag
ord-20c2d38e6ad9416bb3a72c8619235aed
Quelldatensatz
uspto-grants-2012_12
Patentnummer
US08329698B2

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