Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:14]=O)[C:6](=[CH:10][C:11]=1[O:12][CH3:13])[C:7](O)=[O:8].O.[NH2:17][NH2:18]>C(O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:6](=[CH:10][C:11]=1[O:12][CH3:13])[C:7](=[O:8])[NH:18][N:17]=[CH:14]2Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4,5-Dimethoxyphthalaldehydic acid (10 g.) and hydrazine hydrate (2.4 ml.) in ethanol (150 ml.) were heated under reflux for 20 hours during which time a white crystalline solid formed. The mixture was cooled in an ice bath, filtered and the resulting product dried to give crude 6,7-dimethoxyphthalazin-1-one (7 g.). A sample was crystallized from water yielding colorless needles, m.p. 254°-256° C.
Aufarbeitung
- temperatureunder reflux for 20 hours during which time a white crystalline solid
- customformed
- temperatureThe mixture was cooled in an ice bath
- filtrationfiltered
- customthe resulting product dried
Quellen und Nachweise
- ORD-Eintrag
- ord-153785bad39141c4860e60f40756846b
- Quelldatensatz
- uspto-grants-1983_01
- Patentnummer
- US04370328
Verknüpfte Notizen
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