Liquid crystal compound and liquid crystal composition comprising same
A technology of liquid crystal compounds and liquid crystal compositions, applied in the field of liquid crystal compounds and liquid crystal compositions, which can solve problems such as increased rotational viscosity
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preparation example 1
[0118] Preparation Example 1 (FNF-H.O2)
[0119]
[0120] Bromide compound (chemical formula 1-1, 40mmol, 18.8g) was dissolved in anhydrous THF, then stirred at -30°C and potassium tert-butoxide (48.1mmol, 5.4g) was slowly added, and stirred for 30 minutes. The aldehyde compound (Chemical Formula 1-2, 43.7 mmol, 8.13 g) was dissolved in THF at -30°C and added dropwise. After raising the temperature to -10° C. and stirring for 1 hour, a solvent with a ratio of water to toluene of 1:1 was added into the reactor to terminate the reaction. The organic solvent layer was extracted and distilled under reduced pressure, and the resulting solid was separated by column chromatography to obtain an ethene compound (chemical formula 1-3, 60%, 7.1 g). The obtained ethylene compound (chemical formula 1-3, 24mmol, 7.1g) and palladium / activated carbon (10wt%, 1.5g) were dissolved in THF and the ratio of methanol was 1:1 solvent, then reacted in hydrogenation reactor 3 Filter after hours. ...
preparation example 2
[0122] Preparation example 2 (FNAF-H.O2)
[0123]
[0124] Bromide compound (chemical formula 2-1, 40mmol, 18.8g) was dissolved in anhydrous THF, then stirred at -30°C, potassium tert-butoxide (48.1mmol, 5.4g) was slowly added, and stirred for 30 minutes. The aldehyde compound (Chemical Formula 2-2, 43.7 mmol, 11.45 g) was dissolved in THF at -30°C and added dropwise. After raising the temperature to -10° C. and stirring for 1 hour, a solvent with a ratio of water to toluene of 1:1 was added into the reactor to terminate the reaction. The organic solvent layer was extracted and distilled under reduced pressure, and the resulting solid was separated by column chromatography to obtain an ethylene compound (chemical formula 2-3, 57%, 8.5 g). The obtained ethylene compound (chemical formula 2-3, 22.83mmol, 8.5g) and palladium / activated carbon (10wt%, 2.1g) were dissolved in THF and methanol ratio in a solvent of 1:1, and then reacted in a hydrogenation reactor Filter after 3 ...
preparation example 3
[0126] Preparation example 3 (FANF-H.O2)
[0127]
[0128] Bromide compound (chemical formula 3-2, 27.3mmol, 14g) was dissolved in anhydrous THF, then stirred at -30°C, potassium tert-butoxide (32.7mmol, 3.7g) was slowly added, and stirred for 30 minutes. An aldehyde compound (Chemical Formula 3-1, 29.7 mmol, 6.49 g) was dissolved in THF at -30°C and added dropwise. After raising the temperature to -10° C. and stirring for 1 hour, a solvent with a ratio of water to toluene of 1:1 was added into the reactor to terminate the reaction. The organic solvent layer was extracted and distilled under reduced pressure, and the resulting solid was separated by column chromatography to obtain an ethylene compound (chemical formula 3-3, 65%, 6.6 g). The obtained ethylene compound (chemical formula 3-3, 17.7mmol, 6.6g) and palladium / activated carbon (10wt%, 1.65g) were dissolved in THF and methanol ratio as a solvent of 1:1, and then reacted in a hydrogenation reactor Filter after 3 ho...
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