5-Methylisatin → 7-Bromo-5-methylindoline-2,3-dione
Reaktionsgleichung
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6](=[O:11])[C:5]2=[O:12].[Br:13]Br>C(O)(=O)C>[Br:13][C:9]1[CH:10]=[C:2]([CH3:1])[CH:3]=[C:4]2[C:8]=1[NH:7][C:6](=[O:11])[C:5]2=[O:12]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a suspension of 8.0 g of 5-methylisatin in 200 ml of acetic acid was added dropwise a solution of 3.3 ml of bromine in 50 ml of acetic acid with stirring at room temperature, and the mixture was heated at 50° C. for 16 hours. The reaction mixture was concentrated under reduced pressure, and the residue was recrystallized from methanol-hexane to obtain 11.4 g of 7-bromo-5-methylisatin having a melting point of 176°-180° C.
Aufarbeitung
- temperaturethe mixture was heated at 50° C. for 16 hours
- concentrationThe reaction mixture was concentrated under reduced pressure
- customthe residue was recrystallized from methanol-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-e464e95d98324dbe8b7ef8efaf54000c
- Quelldatensatz
- uspto-grants-1988_10
- Patentnummer
- US04780477
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