Liquid crystal compound and application thereof
A liquid crystal compound and liquid crystal composition technology, applied in liquid crystal materials, chemical instruments and methods, optics, etc., can solve the problems of not using liquid crystal composition, etc., and achieve the effects of stable properties, low viscosity, and good mutual solubility
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Embodiment 1
[0027]
[0028] a:n-BuLi,CO 2 ,H 2 O;b:CF 3 SO 3 ,HS(CH 2 ) 3 SH; c: 3,5-difluoro-4-benzyloxyphenol, Et 3 N;d:3HF.Et 3 N;e:Br 2
[0029] Add 0.1 moles of 1-(4-propylcyclohexyl)-2-(3,5-difluorophenyl)propane and 0.2L tetrahydrofuran to the three-necked flask in sequence, cool to -70°C, and slowly drop 0.11 moles of n-butyllithium, keep the temperature for 1 hour after the dropwise addition. Introduce dry carbon dioxide gas until no longer exothermic. 1.0M hydrochloric acid and 1.0L ice water are used for hydrolysis, and the pH value is adjusted to be below 1 after hydrolysis. Add 0.4L of toluene and stir for 5 minutes, let stand for 10 minutes, and separate the liquids. The upper layer is the product phase, washed three times with 0.2L×3 water, and dried with 20g of anhydrous magnesium sulfate for 1 hour. The desiccant was filtered, and the solvent was distilled off to obtain a light yellow solid, which was recrystallized from absolute ethanol to obtain a white s...
Embodiment 2
[0039]
[0040] Synthesis of 5-(4-propylbicyclohexyl)acetyl-1,3-difluorobenzene
[0041]Add 0.48 moles of magnesium chips and 200 milliliters of tetrahydrofuran (THF) successively in the there-necked flask, heat to reflux, add dropwise 20 milliliters of 4-propyl bicyclohexyl methyl bromide and 100 milliliters of tetrahydrofuran (THF) to initiate the reaction. Add the remaining solution dropwise at ℃, continue to reflux for 1 hour, and then add dropwise a solution composed of 0.4 moles of 3,5-difluorobenzonitrile and 300 ml of toluene at 70°C, and reflux for 4 hours after the dropwise addition, then slowly add 500 The ml of 2M hydrochloric acid was refluxed for 2 hours, separated, washed with water until neutral, evaporated to remove the solvent, and recrystallized with 4 times absolute ethanol to obtain 84.8 g of A1 as a white solid. The gas phase purity is 99.2%.
[0042]
[0043] Synthesis of 1-(4-propylbicyclohexyl)-2-(3,5-difluorophenyl)propane
[0044] Add 0.2 mol...
Embodiment 3
[0054] The liquid crystal compound was prepared according to the following components and their proportions, and its properties are shown in Table 1.
[0055] Component Servings
[0056]
[0057]
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