Reaktionsgleichung
[I:1](O)(=O)(=O)=O.[I-:6].[K+].[F:8][C:9]([F:21])([F:20])[C:10]1[CH:15]=[CH:14][C:13]([C:16]([F:19])([F:18])[F:17])=[CH:12][CH:11]=1>OS(O)(=O)=O>[F:8][C:9]([F:20])([F:21])[C:10]1[CH:11]=[C:12]([I:6])[C:13]([C:16]([F:17])([F:18])[F:19])=[CH:14][C:15]=1[I:1]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 70 °C
Versuchsvorschrift
To a solution of 30 mL H2SO4 was added periodic acid (3.18 g, 14 mmol) and potassium iodide (6.90 g, 42 mmol) under ice bath and then 1,4-bis(trifluoromethyl)benzene (2.17 mL, 14 mmol) was added. The reaction mixture was then stirred at 70° C. for 5 h. After cooling down to room temperature, the resulting solution was poured into ice-water and then extracted with diethyl ether (100 mL) and 10% sodium thiosulfate (50 mL). The organic layer was washed with 10% sodium thiosulfate (3×50 mL), dried over MgSO4, filtered, and concentrated. The residue was recrystallized from hexane to give 19 as a white solid (4.24 g, 65%): 1H NMR (300 MHz, CDCl3): δ 8.20 (s, 2H); 19F N (282 MHz, CDCl3): −64.2; HR-MS (EI) calcd. for C8H2F6I2 (M+): 465.81, found: 465.8387.
Aufarbeitung
- temperatureAfter cooling down to room temperature
- extractionextracted with diethyl ether (100 mL) and 10% sodium thiosulfate (50 mL)
- washThe organic layer was washed with 10% sodium thiosulfate (3×50 mL)
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe residue was recrystallized from hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-17cc6316a2af473aa473c6455b19a5ef
- Quelldatensatz
- uspto-grants-2010_04
- Patentnummer
- US07700366B2
Verknüpfte Notizen
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