Reaktionsgleichung
F[C:2]([F:13])(F)[C:3]([O:5][C:6](=[O:11])[C:7]([F:10])([F:9])[F:8])=O.[F:14][C:15]1[C:20]([F:21])=CC(F)=[C:17]([F:23])[C:16]=1O.B(F)(F)F.CCOCC>>[F:10][C:7]([F:8])([F:9])[C:6]([O:5][C:3]1[C:2]([F:13])=[C:17]([F:23])[CH:16]=[C:15]([F:14])[C:20]=1[F:21])=[O:11]Komponenten
4
Versuchsvorschrift
Trifluoroacetic anhydride (28 mL, 0.2 mol) was added dropwise with stirring to 27.1 g (0,163 mol) of 2,3,5,6tetrafluorophenol. Boron trifluoride etherate (0.2 mL) was added and the mixture was refluxed overnight. The residual solution was distilled at atmospheric pressure to remove trifluoroacetic anhydride and trifluoroacetic acid. The desired product 18 (32.2 g; 75% yield) was collected at 45° C. (18mm) as a colorless liquid:
Aufarbeitung
- temperaturethe mixture was refluxed overnight
- distillationThe residual solution was distilled at atmospheric pressure
- customto remove trifluoroacetic anhydride and trifluoroacetic acid
Quellen und Nachweise
- ORD-Eintrag
- ord-0f9b25f93fa74c2990bd28e8b3c03f57
- Quelldatensatz
- uspto-grants-1995_05
- Patentnummer
- US05419966
Verknüpfte Notizen
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