Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfate | HCID 6497 | — |
| Edukt | Cesium fluoride | HCID 25953 | — |
| Edukt | Decafluorocyclohexanone | HCID 12570757 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diglyme | HCID 8150 | — |
| Produkt | Methyl perfluorobutyl ether | HCID 164514 | — |
Reaktionsschritte
A 500 ml, 3-necked round bottom flask equipped with an overhead stirrer, an addition funnel, and a condenser was charged with anhydrous cesium fluoride (27.4 g, 0.18 mole), anhydrous diethylene glycol dimethyl ether (258 g, hereinafter diglyme), and dimethyl sulfate (22.7 g, 0.18 mole). Perfluorocyclohexanone (50 g, 0.18 mole) was then added dropwise to the resulting stirred mixture, and stirring was continued for 18 hours after the addition. Water (approximately 200 ml) was added to the resulting mixture, and the lower fluorochemical phase of the mixture was separated from the upper phase and washed once with saturated aqueous sodium chloride solution. Since the fluorochemical phase still contained about 12% diglyme, water was added to it, and the resulting product was azeotropically distilled to yield 32.8 g of c-C6F11OCH3 (b.p.=100° C.), which was free of diglyme. The product identity was confirmed by IR, GCMS, and 1H and 19F NMR.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06380149B2 |
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| Quelldatensatz | uspto-grants-2002_04 |
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| ORD ID | ord-ea8459e4dffb4d92b86b315d0dd58102 |
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| Quellennotiz | uspto-grants-2002_04 |
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