Reaktionsgleichung
[CH:1]1[C:14]2[S:13][C:12]3[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=3)[S:6][C:5]=2[CH:4]=[CH:3][CH:2]=1.[N+]([O-])(O)=[O:16].O>C(O)(=O)C>[CH:11]1[C:12]2[S:13][C:14]3[C:5](=[CH:4][CH:3]=[CH:2][CH:1]=3)[S:6](=[O:16])[C:7]=2[CH:8]=[CH:9][CH:10]=1Komponenten
5
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In 300 ml of acetic acid was refluxed 20 g of thianthrene and 36 ml of diluted nitric acid was gradually added dropwise thereto. After reacting for 5 hours, the reaction solution was poured into 1.2 liters of water to deposit crystals. The crystals were collected by filtration and recrystallized from acetonitrile to obtain 12 g of thianthrene-S-oxide. 1H-NMR (400 MHz, CDCl3): σ 7.42 (t, 2H), 7.56 (t, 2H), 7.63 (d, 2H), 7.93 (d, 2H).
Aufarbeitung
- additionwas gradually added dropwise
- filtrationThe crystals were collected by filtration
- customrecrystallized from acetonitrile
Quellen und Nachweise
- ORD-Eintrag
- ord-3264c7bb4cc544399726d73203c51db1
- Quelldatensatz
- uspto-grants-2009_11
- Patentnummer
- US07615330B2
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