Reaktionsgleichung
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[CH:4][C:3]=1[F:9].O([CH2:18][C:19]([F:25])([F:24])[C:20]([F:23])([F:22])[F:21])S(C(F)(F)F)(=O)=O.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][CH2:18][C:19]([F:25])([F:24])[C:20]([F:23])([F:22])[F:21])=[CH:4][C:3]=1[F:9]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The title compound was prepared from 4-bromo-3-fluorophenol and 2,2,3,3,3,-pentafluoropropyl triflate with potassium carbonate in acetone at ambient temperature for 18 hours. Kugelrohr distillation provided a colorless oil, b.p. 105-110° C./12 mbar.
Aufarbeitung
- distillationKugelrohr distillation
- customprovided a colorless oil, b.p. 105-110° C./12 mbar
Quellen und Nachweise
- ORD-Eintrag
- ord-7ef815b8595f4da1b115d094560517b9
- Quelldatensatz
- uspto-grants-2013_02
- Patentnummer
- US08367838B2
Verknüpfte Notizen
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