Dibenzothiophene polymerizable compound and application thereof
A technology of dibenzothiophene and compounds, applied in the field of liquid crystal compounds and its applications, can solve the problems of low residue and poor display, etc., and achieve the effects of fast response, good anti-ultraviolet performance, and wide temperature range of nematic phase
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Embodiment 1
[0058] The structural formula of the liquid crystal compound is:
[0059]
[0060] The synthetic route for preparing compound BYLC-01 is as follows:
[0061]
[0062] Specific steps are as follows:
[0063] (1) Synthesis of compound BYLC-01-1:
[0064] Add 40.5g of 3-benzyloxy-7-bromo-4,6-difluorodibenzothiophene, 20g of diethyl malonate, 14g of potassium tert-butoxide, and 300ml of tetrahydrofuran into the reaction flask, and control the temperature at 50°C to 60°C React at ℃ for 6 hours, lower to room temperature, adjust the pH value to neutral with dilute hydrochloric acid, perform conventional post-treatment, and recrystallize to obtain 43.5 g of light yellow solid (compound BYLC-01-1), HPLC: 99.4%, yield 85.0%;
[0065] (2) Synthesis of compound BYLC-01-2:
[0066] Add 10.0g of aluminum hydride and 500mL of tetrahydrofuran into the reaction flask, cool down to 0°C, control the temperature at 0°C to 10°C, add dropwise a solution composed of 43.5g of compound BYLC-...
Embodiment 2
[0074] The structural formula of the liquid crystal compound is:
[0075]
[0076] The synthetic route for preparing compound BYLC-02 is as follows:
[0077]
[0078] Specific steps are as follows:
[0079] Synthesis of compound BYLC-02:
[0080] Under the protection of nitrogen, add 31.0g of compound BYLC-01-3, 38.4g of triethylamine and 250mL of dichloromethane into the reaction flask, cool down to -10°C, control the temperature from -10°C to 0°C, and add 32.0g of acryloyl chloride dropwise, Rise to room temperature and react for 6 hours. Pour the reaction solution into water, neutralize it with aqueous uranium bicarbonate solution, perform conventional post-treatment, purify by chromatography, elute with n-hexane, and recrystallize from ethanol to obtain 38.9 g of a white solid (compound BYLC-02), LC : 99.6%, yield: 82.5%.
[0081] The obtained white solid BYLC-02 was analyzed by GC-MS, and the m / z of the product was 472.1 (M+).
[0082] 1 H-NMR (300MHz, CDCl 3 ...
Embodiment 3
[0084]
[0085] The synthetic route for preparing compound BYLC-03 is as follows:
[0086]
[0087] Specific steps are as follows:
[0088] (1) Synthesis of compound BYLC-03-1:
[0089]Under the protection of nitrogen, add 40.5g 3-benzyloxy-7-bromo-4,6-difluorodibenzothiophene and 300ml tetrahydrofuran into the reaction flask, cool down to -70℃~-80℃, add dropwise 0.13mol n-butyl Lithium base, temperature control -70℃~-80℃, react for 1h, add 18.0g trimethyl borate dropwise, return to -30℃ naturally, acidify with dilute hydrochloric acid to adjust the pH value to less than 2, carry out conventional post-treatment, and recrystallize to obtain shallow Yellow solid (compound BYLC-03-1) 32.3g, LC: 98.5%, yield 87.3%;
[0090] (2) Synthesis of compound BYLC-03-2:
[0091] Add 32.3g of compound BYLC-03-1, 18.5g of p-bromoiodobenzene, 18.0g of anhydrous potassium carbonate, 200ml of toluene, 150ml of ethanol, 150ml of water, 0.3g of tetrakistriphenylphosphine palladium into th...
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