Optically anisotropic layer, method for producing the optically anisotropic layer, a laminate, polarizing plate, display device, liquid crystal compound, method for producing the liquid crystal compound, and carboxylic acid compound
A technology of optical anisotropy and liquid crystal compounds, applied in chemical instruments and methods, optics, liquid crystal materials, etc., can solve problems such as the influence of display characteristics
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Embodiment 1
[0282] Compound (I-1) was synthesized according to the following scheme.
[0283]
[0284]
[0285] Succinic acid mono(2-acryloyloxyethyl) ester (I-1A) 182g (839mmol), ethyl acetate 600mL, N,N-dimethylacetamide 150mL, 2,6-di-tert-butyl- 680 mg of 4-methylphenol was mixed, and the internal temperature was cooled to 5°C. 642 mL (879 mmol) of thionyl chloride was added dropwise to the mixture, taking care not to raise the internal temperature above 10°C. After stirring at 5° C. for 1 hour, a solution of 111 g (800 mmol) of 2-(4-hydroxyphenyl)ethanol in 220 mL of N,N-dimethylacetamide was added. Then, after stirring at room temperature for 12 hours, 400 mL of water was added for liquid separation. The collected organic layer was washed with 1N hydrochloric acid water, saturated sodium bicarbonate water and saturated brine, and dried over anhydrous sodium sulfate. Sodium sulfate was filtered off, and the solvent was removed by a rotary evaporator to obtain 255 g (758 mmol) ...
Embodiment 2
[0296] Compound (I-2) was synthesized according to the following scheme.
[0297]
[0298]
[0299] 40g (307mmol) of 2-hydroxyethyl methacrylate (I-2a), 300mL of dichloromethane, 3.8g (30.7mmol) of N,N-dimethylaminopyridine, 33.8g (338mmol) of succinic anhydride, 2, 200 mg of 6-di-tert-butyl-4-methylphenol was mixed, and the inner temperature was heated to 40°C. After stirring for 12 hours, it was cooled to room temperature, and 300 mL of water was added and stirred for 1 hour for liquid separation. The collected organic layer was washed with 1N hydrochloric acid water and saturated brine, and dried over anhydrous sodium sulfate. Sodium sulfate was filtered off, and the solvent was removed by a rotary evaporator to obtain 64 g (278 mmol) of compound (I-2A) as a clear oil (91% yield).
[0300]
[0301] Mix 30 g (130 mmol) of compound (I-2A), 50 mL of ethyl acetate, 15 mL of N,N-dimethylacetamide, and 100 mg of 2,6-di-tert-butyl-4-methylphenol, and cool the internal tem...
Embodiment 3
[0309] Compound (I-3) was synthesized according to the following scheme.
[0310]
[0311]
[0312] Compound (I-3A) was synthesized in the same manner as in Example 2, except that Compound (I-2a) in the synthesis method of Compound (I-2A) described in Example 2 was changed to Compound (I-3a). The rate is 92%).
[0313]
[0314] Compound (I-3B) was synthesized in the same manner as in Example 1, except that Compound (I-1A) in the synthesis method of Compound (I-1B) described in Example 1 was changed to Compound (I-3A). The rate is 94%).
[0315]
[0316] Compound (I-3C) was synthesized in the same manner as in Example 1, except that Compound (I-1B) in the synthesis method of Compound (I-1C) described in Example 1 was changed to Compound (I-3B). rate of 70%).
[0317] 1 H-NMR (solvent: CDCl 3 )δ (ppm): 1.45-1.72 (m, 4H), 1.72-1.80 (m, 4H), 2.10-2.30 (m, 4H), 2.33-2.45 (m, 1H), 2.47-2.65 (m, 1H) , 2.62(s, 4H), 2.93(t, 2H), 4.10-4.22(m, 4H), 4.30(t, 2H), 5.83(dd, 1H...
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