A kind of preparation method of bisfluorosulfonimide alkali metal salt
A technology of bisfluorosulfonimide base and bischlorosulfonimide base is applied in directions such as nitrogen and non-metallic compounds, sulfamic acid, etc., to solve the problem of sublimation residues, reduce preparation costs, and simplify purification steps.
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Embodiment 1
[0036] The preparation method of bisfluorosulfonimide alkali metal salt, the steps are as follows:
[0037](1) Under the protection of dry nitrogen, add 0.2L dimethyl carbonate and 115g dichlorosulfonimide potassium salt into a 1L three-necked flask. After stirring and dissolving, 148 g of dried bismuth fluoride was added at room temperature, and stirred at room temperature for 24 hours. After the reaction, the system was moved to a glove box with a water content lower than 1 ppm to filter and remove excess bismuth fluoride. The filtrate was evaporated to dryness with a rotary evaporator to obtain a light yellow solid mixture;
[0038] (2) Under the protection of dry nitrogen, the above light yellow solid mixture was dissolved in 120 g of absolute ethanol in a jacketed flask with a cooling device, and the temperature of the solution was kept not higher than 20° C. After stirring and dissolving for 4 hours, it was transferred to a glove box for filtration, and the filtrate wa...
Embodiment 2
[0040] The preparation method of bisfluorosulfonimide alkali metal salt, the steps are as follows:
[0041] (1) Under the protection of dry nitrogen, 0.2 L of acetonitrile and 117.6 g of lithium dichlorosulfonimide were added to a 1 L three-necked flask. After stirring and dissolving, 64 g of dry antimony fluoride was added at room temperature, and the reaction was stirred at room temperature for 24 hours. After the reaction, the system was moved to a glove box with a moisture content lower than 1 ppm to remove excess antimony fluoride by filtration. The filtrate was evaporated to dryness with a rotary evaporator to obtain a light yellow solid mixture;
[0042] (2) Under the protection of dry nitrogen, the above light yellow solid mixture was dissolved in 200 g of anhydrous toluene in a jacketed flask with a cooling device, and the temperature of the solution was kept not higher than 20° C. After stirring and dissolving for 4 hours, it was transferred to a glove box for filt...
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