Synthesis method for bis(fluorosulfonyl)imide salt
A technology of bisfluorosulfonimide salt and bischlorosulfonimide salt, which is applied in the field of halogen exchange fluorination synthesis, can solve the problems of difficult separation and purification operation, inability to remove, cumbersome and the like, and achieves simple process operation and high product quality. The effect of high yield and high product purity
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Embodiment 1
[0022] Embodiment 1: Potassium difluorosulfonimide ([KN(SO 2 F)] 2 , referred to as KFSI) preparation.
[0023] Under nitrogen protection, 504g (2mol) of potassium dichlorosulfonimide (KCSI) was added to a 2000ml three-necked flask; then 900g (10mol) of dimethyl carbonate was added to the three-necked flask, and stirred at room temperature until the solution clarify.
[0024] Under the condition of stirring, 464g (4mol) compound fluorinating agent (wherein antimony trifluoride 23.2g, potassium fluoride 440.8g) is evenly divided into 7 batches, and adjacent batches are added to the above-mentioned 2000ml three-necked flask at intervals of 45 minutes. The temperature was raised to 100° C. and the mixture was stirred and refluxed for 8 hours.
[0025] After the reaction, the reaction solution was filtered to remove insoluble matter, the filtrate was concentrated to 300 g, and cooled to 5° C. to crystallize. Then filter, wash, and dry to obtain 218.6 g (0.998 mol) of potassium...
Embodiment 2
[0026] Embodiment 2: Sodium bisfluorosulfonimide ([NaN(SO 2 F)] 2 , referred to as NaFSI).
[0027]Under nitrogen protection, 472g (2mol) of sodium bischlorosulfonimide (NaCSI) was added to a 2000ml three-necked flask; then 900g (10mol) of dimethyl carbonate was added to the three-necked flask, and stirred at room temperature until the solution clarify.
[0028] Under stirring, 464g (4mol) compound fluorinating agent (wherein antimony trifluoride 23.2g, potassium fluoride 440.8g) is evenly divided into 9 batches, and adjacent batches are added in the above-mentioned 2000ml three-necked flask at intervals of 40 minutes. The temperature was raised to 100° C. and the mixture was stirred and refluxed for 8 hours.
[0029] After the reaction was completed, the reaction solution was filtered to remove insoluble matter, the filtrate was concentrated to 360 g, and cooled to 5° C. for crystallization. Then filter, wash, and dry to obtain 268g (1.32mol) of sodium bisfluorosulfonimid...
Embodiment 3
[0030] Embodiment 3: Lithium difluorosulfonimide ([LiN(SO 2 F)] 2 , referred to as LiFSI).
[0031] Under nitrogen protection, 440g (2mol) of lithium bischlorosulfonimide (LiCSI) was added to a 2000ml three-necked flask; then 900g (10mol) of dimethyl carbonate was added to the three-necked flask, and stirred at room temperature until the solution clarify.
[0032] Under the condition of stirring, 464g (4mol) compound fluorinating agent (wherein antimony trifluoride 23.2g, potassium fluoride 440.8g) is evenly divided into 10 batches, and adjacent batches are added in the above-mentioned 2000ml three-necked flask at intervals of 50 minutes, The temperature was raised to 100° C. and the mixture was stirred and refluxed for 8 hours.
[0033] After the reaction was completed, the reaction solution was filtered to remove insoluble matter, the filtrate was concentrated to 360 g, and cooled to 5° C. for crystallization. Then filtered, washed, and dried to obtain 195 g (1.04 mol) o...
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