Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfate Ion | HCID 1117 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 3,4,5,6-Tetrafluorophthalic acid | HCID 69544 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1,2,3,4-Tetrafluorobenzene | HCID 11084 | — |
| Produkt | 2,3,4-Trifluorophenol | HCID 123174 | — |
Reaktionsschritte
In an autoclave having an inner volume of 100 ml, 3.0 g (0.0126 mole) of 3,4,5,6-tetrafluorophthalic acid containing no sulfate ion, 0.5 g (0.0125 mole) of sodium hydroxide, and 50 g of water were placed and heated for reaction at 200° C. for 25 hours. After completion of the reaction, the reaction mixture was cooled to room temperature and extracted with 150 ml of diisopropyl ether. By analyzing this extract by gas chromatography using a 2 m column packed with SE52 and kept at 50° C., the reaction was found to have produced 2.9 mole % of 1,2,3,4-tetrafluorobenzene, 89.1 mole % of trifluorophenol, and substantially no 2,3,4,5-tetrafluorobenzoic acid based on the 3,4,5,6-tetrafluorophthalic acid used as the starting material [pH 2.75 at 25° C. at the time of charging].
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04769492 |
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| Quelldatensatz | uspto-grants-1988_09 |
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| ORD ID | ord-cd5760b79d004bedb9f906022f11db42 |
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| Quellennotiz | uspto-grants-1988_09 |
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