Polymerizable compound containing benzothiophene
A technology for polymerizing compounds and compounds, applied in the fields of organic chemistry, chemical instruments and methods, instruments, etc., can solve the problems of poor uniformity and low TFT display, and achieve the effects of less monomer residue, high charge retention rate, and high polymerization activity.
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Embodiment 1
[0084] step one
[0085] Add 0.056mol (1-a) 15.12g and dichloromethane 200g into a 500ml three-necked flask, cool the reaction solution to 0-5°C, drop 0.067mol16.87g of boron tribromide, and react overnight.
[0086] The reaction solution was poured into a beaker filled with 500g of water, and separated. The aqueous phase was extracted three times with 300 g of dichloromethane. The organic phase was washed twice with 300 g of water. The organic phase was evaporated to dryness to obtain 12.1 g of product 1-b, yield: 89.3%
[0087] Jump straight into the next step.
[0088] Gc-MS: see attached picture 1
[0089] step two
[0090]
[0091] Add 0.05mol1-b12.1g, 250g of dichloromethane, 0.6g of DMAP, 27g of DCC, 11g of methacrylic acid into a 500ml three-necked flask, and react overnight at 25°C.
[0092]The reaction solution was poured into a beaker filled with 500g of water, and separated. The aqueous phase was extracted three times with 250 g of dichloromethane. The...
Embodiment 2
[0095]
[0096] Add 0.05mol1-b12.1g, 250g of dichloromethane, 0.6g of DMAP, 27g of DCC, 15g of trifluoromethacrylic acid into a 500ml three-necked flask, and react overnight at 25°C.
[0097] The reaction solution was poured into a beaker filled with 500g of water, and separated. The aqueous phase was extracted three times with 250 g of dichloromethane. The organic phase was washed twice with 250 g of water.
[0098] The solvent was evaporated to dryness under reduced pressure, dissolved in toluene, passed through a silica gel chromatography column, and the solvent was evaporated to dryness. Toluene was recrystallized 3 times. 12.5 g of I-2 was obtained, yield 51%, Gc: 99.81%.
[0099] The compounds of Examples I-1 and I-2 have the advantage of longer ultraviolet absorption wavelengths, which can reduce damage to liquid crystal molecules during the process of forming an alignment layer by ultraviolet irradiation polymerization.
Embodiment 3
[0101]
[0102]
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