Electrolyte containing saturated heterocycles and preparation and application thereof
A technology of electrolytes and heterocycles, applied in the field of electrolytes containing saturated heterocycles, can solve problems such as correlation or deducibility uncertainty, achieve the effects of inhibiting electrolyte decomposition, high ion conductivity, and improving cycle performance
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Embodiment 1
[0063] Embodiment 1: raw material
[0064] Preparation method: Under nitrogen atmosphere, the raw material 2,5-difluoro-1,1-dimethylsiloxane-3,4-diol (1.34g, 0.01mol) and boron trifluoride tetrahydrofuran complex ( 2.8g, 0.02mol) were mixed uniformly in 15ml of ethylene glycol dimethyl ether, and reacted at room temperature for 12 hours. The obtained mixed solution was dried under reduced pressure at 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Dissolve lithium ethoxide (1.04g, 0.02mol) in 10ml of ethanol and slowly add it to the intermediate, stir and react at 45°C for 8 hours, and dry the resulting mixture under reduced pressure at 40°C and vacuum degree of about -0.1MPa , The obtained solid was washed three times with n-butyl ether, filtered and dried to obtain the product M1. Yield was 78%, NMR as figure 1 shown.
Embodiment 2
[0065] Embodiment 2: raw material
[0066]Preparation method: Under an argon atmosphere, the raw material 2,2-difluoro-1,3-bis(hydroxymethyl)-5,5-dimethylimidazolin-4-one (2.1g, 0.01mol) and three Boron fluoride diethyl ether complex (2.98g, 0.021mol) was mixed uniformly in 15ml of ethylene glycol dimethyl ether, and reacted at room temperature for 12 hours. The resulting mixed solution was dried under reduced pressure at 30° C. and a vacuum of about −0.1 MPa to remove the solvent to obtain an intermediate. Add 14ml of butyllithium hexane solution (c=1.6mol / L) to the intermediate, stir and react at room temperature for 6 hours, and dry the resulting mixture under reduced pressure at 40°C and a vacuum of about -0.1MPa. The obtained crude product was washed 3 times with cyclohexane, filtered and dried to obtain the product M2. The yield was 87%, NMR such as figure 2 shown.
Embodiment 3
[0067] Embodiment 3: raw material
[0068] Preparation method: Under a nitrogen atmosphere, take the raw materials N-Boc-cis-4-hydroxypyrrolidine-2-carboxylic acid (2.31g, 0.01mol) and lithium methoxide (0.76g, 0.02mol), mix them with 20ml of methanol, Reaction at room temperature for 8 hours. The obtained mixed solution was dried under reduced pressure at 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Add boron trifluoride tetrahydrofuran complex (3.07g, 0.022mol) and 10ml THF to the intermediate, stir and react at room temperature for 6 hours, and depressurize the resulting mixture at 40°C and a vacuum of about -0.1MPa After drying, the resulting solid was washed three times with isopropyl ether, filtered and dried to give the product M3. Yield 77%, NMR as image 3 shown.
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