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HRID 1985579Erstellt: 26. Oktober 2026
Potassium 1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonate → HCID 178448554, Verbindung
https://huagongshe.com/reaction/1985579
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium 1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonate | HCID 87095932 | — |
| Edukt | HCID 178448538 | HCID 178448538 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 178448554 | HCID 178448554 | 67,8% |
Reaktionsschritte
1-Butyl-3-methylimidazolium chloride (Bmim-Cl, 10.0 g) and deionized water (15 ml) were combined at room temperature in a 200 ml flask. At room temperature in a separate 200 ml flask, potassium 1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonate (TTES-K, 16.4 g) was dissolved in deionized water (90 ml). These two solutions were combined at room temperature and allowed to stir magnetically for 30 min. under positive nitrogen pressure to give a biphasic mixture with the desired ionic liquid as the bottom phase. The layers were separated, and the aqueous phase was extracted with 2×50 ml portions of methylene chloride. The combined organic layers were dried over magnesium sulfate and concentrated in vacuo. The colorless oil product was dried at for 4 hr at 5 Pa and 25° C. to afford 15.0 g of product.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07544813B2 |
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| Quelldatensatz | uspto-grants-2009_06 |
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| ORD ID | ord-6624c5a803d9486b8ea6a584016e8154 |
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| Quellennotiz | uspto-grants-2009_06 |
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