Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]([CH3:13])[CH3:12])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[I:14]I>CCO.S([O-])([O-])(=O)=O.[Ag+2]>[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]([CH3:13])[CH3:12])(=[O:10])=[O:9])=[CH:4][C:3]=1[I:14]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Reaktionsbedingungen
- Temperatur
- 50 °C
Versuchsvorschrift
To a stirred solution of 4-amino-N,N-dimethylbenzenesulfonamide (3.0 g, 14.98 mmol) in EtOH (165 mL) at 50° C. was added a slurry of iodine (1.3 g, 4.99 mmol) and silver sulfate (2.8 g, 9.00 mmol) in EtOH (40 mL). The same addition was repeated after 1 h of stirring at 50° C., then the reaction mixture was stirred at 50° C. for 16 h. Iodine (0.76 g, 3.00 mmol) was again added, and the mixture stirred at 50° C. for 2 h before being filtered through Celite®. The filtrate was concentrated in vacuo, and EtOH (70 mL) was added. The suspension was stirred at 50° C. for 1 h, cooled to r.t., then filtered to give the title compound (2.7 g, 55%) as a brown solid that was used without further purification. δH (DMSO-d6) 7.81 (1H, d, J 2.1 Hz), 7.42 (1H, dd, J 8.6 and 2.1 Hz), 6.83 (1H, d, J 8.6 Hz), 6.12 (2H, br. s), 2.58 (6H, s). LCMS (ES+) 326.9 (M+H)+, RT 2.50 minutes (Method 3).
Aufarbeitung
- additionThe same addition
- stirringthe reaction mixture was stirred at 50° C. for 16 h
- stirringthe mixture stirred at 50° C. for 2 h
- filtrationbefore being filtered through Celite®
- concentrationThe filtrate was concentrated in vacuo, and EtOH (70 mL)
- additionwas added
- stirringThe suspension was stirred at 50° C. for 1 h
- temperaturecooled to r.t.
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-8c6efc0a8e54436eaf6468697e075fea
- Quelldatensatz
- uspto-grants-2012_08
- Patentnummer
- US08242116B2
Verknüpfte Notizen
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