Reaktionsgleichung
[C:1]([C:3]1[C:12]([C:13]#[N:14])=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=1)#[N:2].C[O-].[Na+].[NH3:18]>CO>[NH:14]=[C:13]1[C:12]2[CH:11]=[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]3=[CH:4][C:3]=2[C:1](=[NH:18])[NH:2]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In 2.5 moles of 2,3-dicyanonaphthalene, 0.075 mole of sodium methoxide and 1 liter of methanol, an ammonia gas was flowed with a suitable flow rate for 40 minutes. Then, the reaction solution was refluxed with heating while flowing the ammonia gas for 4 hours. After cooling, the product was filtered, and recrystallized from a mixed solvent of methanol/ether to yield yellow 1,3-diiminobenz(f)isoindoline in 66% yield.
Aufarbeitung
- temperatureThen, the reaction solution was refluxed
- temperaturewith heating
- customfor 4 hours
- temperatureAfter cooling
- filtrationthe product was filtered
- customrecrystallized from a mixed solvent of methanol/ether
Quellen und Nachweise
- ORD-Eintrag
- ord-38e578938dce4dfbae253f92a8e8872b
- Quelldatensatz
- uspto-grants-1995_06
- Patentnummer
- US05428152
Verknüpfte Notizen
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