Diethyl Oxalate → 5,6,7,8-Tetrachloro-1,4-dihydro-2,3-quinoxalinedione

HRID 53715Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 53715
[C:1]([O:8]CC)(=O)[C:2]([O:4]CC)=O.[NH2:11][C:12]1[C:17]([Cl:18])=[C:16]([Cl:19])[C:15]([Cl:20])=[C:14]([Cl:21])[C:13]=1[NH2:22]>>[Cl:18][C:17]1[C:16]([Cl:19])=[C:15]([Cl:20])[C:14]([Cl:21])=[C:13]2[C:12]=1[NH:11][C:2](=[O:4])[C:1](=[O:8])[NH:22]2

Komponenten

3

Edukt 2

HCID 7268Diethyl OxalateHCID 2817911,2-Diamino-3,4,5,6-tetrachlorobenzene

Produkt 1

HCID 3337015,6,7,8-Tetrachloro-1,4-dihydro-2,3-quinoxalinedione

Versuchsvorschrift

5,6,7,8-Tetrachloro-1,4-dihydro-2,3-quinoxalinedione was prepared using an adaptation of the method of Cheeseman. (Cheeseman, G. W. H. J. Chem. Soc. 1171 (1962)). A mixture of diethyl oxalate (2.97 g, 20.0 mmol) and 1,2-diamino-3,4,5,6-tetrachlorobenzene (500 mg, 2.03 mmol) was heated to reflux under N2 for 6 h. The reaction was allowed to cool to room temperature and the orange solid collected by vacuum filtration and rinsed with cold EtOH (10 mL) and air dried. This solid was recrystallized from abs. ethanol to give 97.0 mg (16%) of an orange solid mp 326°-328° C. (dec). (Lit., >360° ). FT-IR: 3198, 3135 cm-1 (N-H), 1750, 1623 cm-1 (C=O). 1H NMR δ (d6 -DMSO) δ 11.7 (br s, 2H, N-H) EIMS m/z 306 (M+8, 1.7), 304 (M+6, 11.5), 302 (M+4, 47.4), 300 (M+2, 93.9), 288 (M+, 76.7), 274 (50.0), 272 (bp), 270 (79.0), 209 (61.0), 207 (64.0). EIHRMS calc. for C8H2Cl4N2O2 297.8870, found 297.8864.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureto reflux under N2 for 6 h
  3. filtrationthe orange solid collected by vacuum filtration
  4. washrinsed with cold EtOH (10 mL) and air
  5. customdried
  6. customThis solid was recrystallized from abs

Quellen und Nachweise

ORD-Eintrag
ord-4b986a9651e54d9d99b39cfcb7edab99
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05620979

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