Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1985579Generated: October 25, 2026

Potassium 1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonate → HCID 178448554, compound

https://huagongshe.com/reaction/1985579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium 1,1,2-trifluoro-2-(trifluoromethoxy)ethanesulfonateHCID 87095932—
ReactantHCID 178448538HCID 178448538—
SolventWaterHCID 962—
ProductHCID 178448554HCID 17844855467.8%

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° C. to afford 15.0 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544813B2
Source datasetuspto-grants-2009_06
ORD IDord-6624c5a803d9486b8ea6a584016e8154
Source noteuspto-grants-2009_06