Saturated carbocyclic electrolyte and preparation and application thereof
An electrolyte and carbon ring technology, which is applied in circuits, electrical components, secondary batteries, etc., can solve problems such as not much achievement, strong sense of existence, and low reference value, so as to improve electrochemical performance and inhibit electrolyte decomposition , the effect of excellent electrochemical performance
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Embodiment 1
[0065] Example 1: Raw materials
[0066] Preparation method: Under nitrogen atmosphere, the raw materials (1R,2R)-1,2-cyclooctanediol (1.44g, 0.01mol) and boron trifluoride tetrahydrofuran complex (2.8g, 0.02mol) were mixed in 15ml ethyl acetate Glycol dimethyl ether was mixed uniformly, and the reaction was carried out at room temperature for 12 hours. The obtained mixed solution was dried under reduced pressure under the conditions of 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. Lithium ethoxide (1.04g, 0.02mol) was dissolved in 10ml of ethanol and slowly added to the intermediate, the reaction was stirred at 45°C for 8 hours, and the resulting mixture was dried under reduced pressure at 45°C and a vacuum of about -0.1MPa. , the obtained solid was washed three times with n-butyl ether, filtered and dried to obtain the product M1. The yield was 77%, NMR as figure 1 shown.
Embodiment 2
[0067] Example 2: Raw materials
[0068]Preparation method: under argon atmosphere, the raw material cycloheptane-1,4-diol (1.30g, 0.01mol) and boron trifluoride ether complex (2.98g, 0.021mol) were mixed uniformly, and reacted at room temperature for 12 hours , to obtain an intermediate. 14ml of butyllithium in hexane solution (c=1.6mol / L) was added to the intermediate, the reaction was stirred at room temperature for 6 hours, and the resulting mixed solution was dried under reduced pressure at 40°C and a vacuum degree of about -0.1MPa, The obtained crude product was washed three times with cyclohexane, filtered and dried to obtain product M2. The yield was 88%, NMR as figure 2 shown.
Embodiment 3
[0069] Example 3: Raw materials
[0070] Preparation method: under nitrogen atmosphere, take a certain amount of raw material cis-1,5-cyclooctanediol (1.44g, 0.01mol) and lithium methoxide (0.76g, 0.02mol), mix with 20ml methanol, and react at room temperature for 8 hours . The obtained mixed solution was dried under reduced pressure under the conditions of 40° C. and a vacuum degree of about -0.1 MPa to remove the solvent to obtain an intermediate. The boron trifluoride tetrahydrofuran complex (3.07g, 0.022mol) and 15ml THF (tetrahydrofuran) were added to the intermediate, and the reaction was stirred at room temperature for 6 hours. Drying under reduced pressure, the obtained solid was washed three times with isopropyl ether, filtered and dried to obtain product M3. Yield 76%, NMR as image 3 shown.
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