HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045257Generated: October 25, 2026
Potassium 1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonate → HCID 178448554, compound
https://huagongshe.com/reaction/1045257
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium 1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonate | HCID 87095932 | — |
| Reactant | HCID 178448538 | HCID 178448538 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178448554 | HCID 178448554 | 67.8% |
Reaction Steps
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 degrees C. to afford 15.0 g of product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08568608B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-deda7b2317ae4007b266a20673c4ecb9 |
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| Source note | uspto-grants-2013_10 |
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