Reaktionsgleichung
[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][C:8](=[O:11])[C:7]2=O.O.NN>>[CH3:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][C:8](=[O:11])[CH2:7]2Komponenten
3
Versuchsvorschrift
5.00 g (31.0 mmol) 7-methyl-1H-indol-2,3-dione in 18.1 mL (372 mmol) hydrazine hydrate were heated to 110° C. for 3 h. Then the reaction mixture was cooled, the precipitate formed was suction filtered and washed with water. The precipitate was suspended in water, acidified with conc. hydrochloric acid and stirred for 10 min. Then the reaction mixture was stirred for a further 30 min in the ice bath, the precipitate was suction filtered, washed with water and dried.
Aufarbeitung
- temperatureThen the reaction mixture was cooled
- customthe precipitate formed
- filtrationfiltered
- washwashed with water
- stirringThen the reaction mixture was stirred for a further 30 min in the ice bath
- filtrationfiltered
- washwashed with water
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-359fa9febe914ddb907f15fe88f97ad9
- Quelldatensatz
- uspto-grants-2014_01
- Patentnummer
- US08629137B2
Verknüpfte Notizen
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