Imidazole two-functionized room temperature inonic liquid and its preparing method
A room temperature ionic liquid, functionalized technology, applied in organic chemistry and other directions, can solve the problem that bifunctional room temperature ionic liquid has not been reported, and achieve the effects of good electrochemical properties, good thermal stability, and high specific heat capacity.
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Embodiment 1
[0026] Synthesis of N-propionitrile, N'-butyronitrile imidazolium chloride salt
[0027] Weigh 17.02 g (0.25 mol) of imidazole and dissolve it in anhydrous methanol. After stirring at room temperature to fully dissolve it, add 13.27 g of acrylonitrile (0.25 mol) to the above solution, and continue the reaction for 24 h under magnetic stirring at 70 ° C. Then 25.90 g of chloro-n-butyronitrile (0.25 mol) was added to the above solution, the temperature was raised to 80° C. to continue the reaction for 48 hours, the solvent methanol was removed by rotary evaporation, and after cooling to room temperature, 60 ml of ether was added to wash (three times), and the Separate the lower layer of the clear night from the funnel, and vacuumize it under magnetic stirring at 120°C to obtain a light yellow product N-propionitrile, N'-butyronitrile imidazolium chloride salt, which is stable to water and air, with a yield of 87.9%, and a melting point of It is -13.76°C, the density is 1.236g / ml...
Embodiment 2
[0029] Synthesis of N-propionitrile, N'-butyronitrile imidazolium tetrafluoroborate
[0030] Weigh 17.02 g (0.25 mol) of imidazole and dissolve it in anhydrous methanol. After stirring at room temperature to fully dissolve it, add 13.27 g of acrylonitrile (0.25 mol) to the above solution, and continue to react for 24 h under magnetic stirring at 70 ° C, then Add 25.90 g of chloro-n-butyronitrile (0.25 mol) to the above solution, raise the temperature to 80 ° C and continue the reaction for 48 hours, remove the solvent methanol by rotary evaporation, add 60 ml of diethyl ether to wash after cooling to room temperature (three times), use a separatory funnel Separate the lower clear layer and vacuumize it under magnetic stirring at 120°C to obtain a light yellow viscous liquid. Add 200ml of acetone to the ionic liquid prepared above, stir at room temperature to fully dissolve it, add 32.94g of sodium tetrafluoroborate (0.30mol) to the above solution, mechanically stir at room tem...
Embodiment 3
[0032] Synthesis of N-propionitrile, N'-butyronitrile imidazolium hexafluorophosphate
[0033]Weigh 17.02 g (0.25 mol) of imidazole and dissolve it in anhydrous methanol. After stirring at room temperature to fully dissolve it, add 13.27 g of acrylonitrile (0.25 mol) to the above solution, and continue to react for 24 h under magnetic stirring at 70 ° C, then Add 25.90 g of chloro-n-butyronitrile (0.25 mol) to the above solution, raise the temperature to 80 ° C and continue the reaction for 48 hours, remove the solvent methanol by rotary evaporation, add 60 ml of diethyl ether to wash after cooling to room temperature (three times), use a separatory funnel Separate the lower clear layer and vacuumize it under magnetic stirring at 120°C to obtain a light yellow viscous liquid. Add 200ml of deionized water to the ionic liquid prepared above, stir at room temperature to fully dissolve it, add 48.9g of ammonium hexafluorophosphate (0.30mol) to the above solution, and continue to r...
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