Cyclohexane derivatives, preparation method thereof and applications thereof
A kind of technology of mixture and compound, applied in the field of cyclohexane derivative and preparation thereof
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Embodiment 1
[0149] Compound of Example 1 Synthesis of (I-17)
[0150]
[0151] Step 1 (Ⅰ-17-a) Synthesis
[0152] Add 56.64g (0.24mol) 1,4-dibromobenzene (reactant) and 400ml dry tetrahydrofuran (solvent) to a 1L three-necked flask. ) n-butyllithium (reactant), keep it warm for 1 hour after dropping, at the same temperature, add dropwise a mixed solution of 0.216mol 3-methylcyclohexanone (reactant) and 50ml dry tetrahydrofuran (solvent), and stir for 30 minutes after dropping , naturally warming up, 200ml of saturated ammonium chloride aqueous solution was added dropwise at about 0°C (to adjust the pH value), the liquid was separated, the aqueous phase was extracted with 200ml of ethyl acetate (solvent), the organic phase was washed with water, and spin-dried to obtain 50g (GC: 89% ) liquid, add 50g of the product obtained above, 500ml of dry dichloromethane (solvent) into another 1L three-necked bottle, under nitrogen protection, cool down to -25°C, add dropwise 63.3ml (0.397mol,...
Embodiment 2
[0169] Synthesis of (Ⅰ-18)
[0170]
[0171] step 1 Synthesis of (I-18-a)
[0172] Add 75g (0.24mol) of 1,4-dibromobiphenyl (reactant) and 400ml of dry tetrahydrofuran (solvent) into a 1L three-necked flask. N) n-butyllithium (reactant), keep warm for 1 hour after dropping, at the same temperature, add dropwise a mixed solution of 0.216mol 3-methylcyclohexanone (reactant) and 50ml dry tetrahydrofuran (solvent), and stir for 30 Minutes, heat up naturally, add 200ml of saturated ammonium chloride aqueous solution dropwise at about 0°C (adjust the pH value), separate the liquid, extract the aqueous phase with 200ml of ethyl acetate (solvent), wash the organic phase with water, and spin dry to obtain 70g (GC: 89 %) liquid, add 70g of the product obtained above, 500ml of dry dichloromethane (solvent) to another 1L three-necked bottle, under nitrogen protection, cool down to -25°C, add dropwise 63.3ml (0.397mol, 2.2eq) triethyl Silicon hydrogen (reactant), after dropping, a...
Embodiment 3
[0194] Embodiment 3, preparation liquid crystal mixture a
[0195] Mix the compounds uniformly according to the following mass percentages to obtain liquid crystal mixture a:
[0196]
[0197]
[0198] The performance test result of this liquid crystal mixture is as follows:
[0199] Cp: 88°C
[0200] Δn: 0.105
[0201] Δε: 7.3
[0202] gamma 1 :66;
[0203] It can be known from the above that the composition has a high clearing point, appropriate optical anisotropy, low rotational viscosity and fast response speed, and can be suitable for liquid crystal displays.
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