Nitric Acid → Benzothiazole, 2-methyl-6-nitro-
Reaktionsgleichung
[CH3:1][C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[N:6]=1.[N+:11]([O-])([OH:13])=[O:12]>S(=O)(=O)(O)O>[CH3:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([N+:11]([O-:13])=[O:12])[CH:8]=[CH:7][C:5]=2[N:6]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2-Methylbenzothiazole (22 g) in conc. sulfuric acid (80 ml) was cooled to −5° C. A mixture of conc. sulfuric acid (12 ml) in conc. nitric acid (20 ml) was added so as to maintain the temperature below 5° C. (ca. 1.5 hours). After this time the mixture was allowed to warm to room temperature and the solution poured onto ice to give a yellow precipitate. The solid was removed by filtration and recrystallised from ethanol. After filtration the solid was washed with ethanol and dried in a vacuum oven to give 18 g of the desired product.
Aufarbeitung
- additionwas added so as
- temperatureto maintain the temperature below 5° C. (ca. 1.5 hours)
- additionthe solution poured onto ice
- customto give a yellow precipitate
- customThe solid was removed by filtration
- customrecrystallised from ethanol
- filtrationAfter filtration the solid
- washwas washed with ethanol
- customdried in a vacuum oven
Quellen und Nachweise
- ORD-Eintrag
- ord-87f7fa9d6aaf40ab95bf44e71d90cf1f
- Quelldatensatz
- uspto-grants-2009_08
- Patentnummer
- US07579140B2
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