Fluorine-containing acrylate monomer and preparation method and application thereof
A technology of acrylate and monomer, which is applied in the field of fluorine-containing acrylate monomer and its preparation and application, to achieve the effect of simple intermediate process, convenient operation, and avoiding high persistence and accumulation
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Embodiment 1
[0024] Add 50 mL of 1,2-dichloroethane, 17.4 g (0.1 mol) of 2,4-TDI, 1.9 g (0.008 mol) of tetraethyltin, and 0.5 g of hydroquinone into a 250 mL four-necked flask as a polymerization inhibitor, Stir, heat up to 75°C, add dropwise 13.0 g (0.1 mol) of hydroxyethyl methacrylate, after the dropwise addition, TLC detection, follow the reaction progress, keep the temperature and stir for 4 hours. 53.6 g (0.1 mol) of 2-methoxy-3-perfluorononenyloxypropanol was added dropwise. After the dropwise addition was completed, TLC detection was carried out to track the reaction progress, and the reaction was carried out while maintaining the temperature and stirring for 5 h. The reaction is completed, distillation and desolvation, silica gel column chromatography separation (V 环己烷 :V 乙酸乙酯 = 7: 3), the yellow paste I was obtained after removing the solvent 1 (n=9, R is CH 3 ), yield 66.0%, purity 99.8%.
[0025] FT-IR (cm -1): 3324, 2957, 2927, 1709, 1601, 1530, 1276, 1196, 1159, 1080, 80...
Embodiment 2
[0029] React according to the method of Example 1, but 2-methoxyl-3-perfluorononenyloxypropanol is changed to 2-methoxyl-3-perfluorohexenyloxypropanol 38.6g (0.1mol), Other conditions are identical with embodiment 1, obtain pale yellow paste I 2 (n=6, R is CH 3 ), yield 70.1%, purity 99.7%.
[0030] 19 F NMR δ(CDCl 3 ): -129.4(t, 3F), -127.4(s, 3F), -121.6(m, 2F), -83.3(s, 2F), -78.1(t, 1F).
Embodiment 3
[0032] Carry out reaction according to embodiment 1 method, but hydroxyethyl methacrylate is changed into hydroxyethyl acrylate 11.6g (0.1mol), other conditions are identical with embodiment 1, obtain yellow paste I 3 (n=9, R is H), the yield is 69.9%, and the purity is 99.4%.
[0033] 1 H NMR δ(CDCl 3 ): 7.82(s, 1H), 7.21(s, 1H), 7.11(d, 1H), 6.80(s, 1H), 6.50(s, 1H), 6.25(s, 1H), 6.10(s, 1H) , 5.60(s, 1H), 5.08(m, 1H), 4.40(m, 4H), 4.19(m, 2H), 3.60(m, 2H), 3.40(s, 3H), 2.10(s, 3H).
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