Hydrazine → 5-bromo-6-p-tolylpyridazin-3(2H)-one
Reaktionsgleichung
Br[C:2]1[C:3](=O)[O:4][CH:5]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)[C:6]=1[Br:7].[NH2:16][NH2:17]>C(O)C>[Br:7][C:6]1[C:5]([C:8]2[CH:13]=[CH:12][C:11]([CH3:14])=[CH:10][CH:9]=2)=[N:17][NH:16][C:3](=[O:4])[CH:2]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a mixture of 3,4-dibromo-5-p-tolylfuran-2(5H)-one (0.5 g, 1.506 mmol) in ethanol (5 mL) was added NH2NH2 (0.047 mL, 1.506 mmol) at 0° C. The mixture was stirred at room temperature overnight. The precipitate was filtered and dried under reduced pressure to give the title compound as a beige solid (0.22 g). LCMS m/z=264.9 [M+H]+.
Aufarbeitung
- filtrationThe precipitate was filtered
- customdried under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-fd39aa5fc7124ab48029a7f952bd51e1
- Quelldatensatz
- uspto-grants-2015_01
- Patentnummer
- US08940891B2
Notizen zur Reaktion
Wird geladen…