2,3,6-Trichloroquinoxaline → 2,6-Dichloro-6-hydrazinoquinoxaline
Reaktionsgleichung
[Cl:1][C:2]1[C:11](Cl)=[N:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Cl:13])[CH:8]=2)[N:3]=1.O.[NH2:15][NH2:16]>C(O)C>[Cl:1][C:2]1[CH:11]=[N:10][C:9]2[CH2:8][C:7]([Cl:13])([NH:15][NH2:16])[CH:6]=[CH:5][C:4]=2[N:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture consisting of 23 g. (0.10 mole) of 2,3,6-trichloroquinoxaline and 11 g. (0.22 mole) of hydrazine hydrate in 500 ml. of ethanol was stirred at room temperature (~20° C.) overnight (~16 hours). The precipitate which formed was separated by filtration and washed with ethanol to ultimately afford 22.2 g. (97%) of pure 2,6-dichloro-3-hydrazinoquinoxaline, m.p. <250° C. Mass Spectrum: m/e, 228 (P).
Aufarbeitung
- customThe precipitate which formed
- customwas separated by filtration
- washwashed with ethanol to ultimately afford 22.2 g
Quellen und Nachweise
- ORD-Eintrag
- ord-07498c12488a4146a7111ebf04e90bc3
- Quelldatensatz
- uspto-grants-1985_01
- Patentnummer
- US04495187
Notizen zur Reaktion
Wird geladen…