Sodium Carbonate → Tetrafluorophthalic anhydride
Reaktionsgleichung
F[C:2]1(F)[C:10]2[C:5](=[C:6]([F:14])[C:7]([F:13])=[C:8]([F:12])[C:9]=2[F:11])[C:4](=[O:15])[O:3]1.C(=O)([O-])[O-:18].[Na+].[Na+]>>[F:11][C:9]1[C:8]([F:12])=[C:7]([F:13])[C:6]([F:14])=[C:5]2[C:4](=[O:15])[O:3][C:2](=[O:18])[C:10]=12Komponenten
3
Versuchsvorschrift
Into a 500 ml glass reactor equipped with a reflux condenser and a stirrer, 100 g (0.413 mol) of the 3,3,4,5,6,7-hexafluoro-1-[3H]-isobenzofuranone separated by distillation from the mixture of Example 2, and 43.8 g (0.413 mol) of sodium carbonate were charged, and the mixture was reacted at 130° C. for 8 hours with vigorous stirring. Then, the reaction mixture was separated by distillation to obtain 79.5 g of tetrafluorophthalic anhydride. The yield was 87.5%.
Aufarbeitung
- customInto a 500 ml glass reactor equipped with a reflux condenser and a stirrer
- additionwere charged
- customthe mixture was reacted at 130° C. for 8 hours with vigorous stirring
- customThen, the reaction mixture was separated by distillation
Quellen und Nachweise
- ORD-Eintrag
- ord-47fdf145a216466fac5009a275513d91
- Quelldatensatz
- uspto-grants-1996_06
- Patentnummer
- US05523476
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