Reaktionsgleichung
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].[N+:11]([O-])([OH:13])=[O:12]>S(=O)(=O)(O)O>[N+:11]([C:6]1[CH:5]=[C:4]2[C:9](=[CH:8][CH:7]=1)[NH:1][C:2](=[O:10])[CH2:3]2)([O-:13])=[O:12]Komponenten
4
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
2-Oxindole (6.5 g) was dissolved in concentrated sulfuric acid (25 ml) and the mixture maintained at −10 to 15° C. while fuming nitric acid (2.1 ml) was added dropwise. After the addition of the nitric acid the reaction mixture was stirred at 0° C. for 0.5 hour and poured into ice-water. The precipitate which formed was collected by filtration, washed with water and crystallized from 50% acetic acid. The final crystalline product was then filtered, washed with water and dried under vacuum to give 6.3 g (70%) of 5-nitro-2-oxindole.
Aufarbeitung
- additionwas added dropwise
- customThe precipitate which formed
- filtrationwas collected by filtration
- washwashed with water
- customcrystallized from 50% acetic acid
- filtrationThe final crystalline product was then filtered
- washwashed with water
- customdried under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-a25b5c81766e4b1da1007624f5d595d1
- Quelldatensatz
- uspto-grants-2005_02
- Patentnummer
- US06855730B2
Verknüpfte Notizen
Wird geladen…