Acrylamide copolymer containing halothane and phosphoric acid ester as well as preparation method and application thereof
A technology of acrylamide copolymer and fluorine-containing alkyl phosphonate, which is applied in the direction of plant fiber, textile and papermaking, fiber treatment, etc., and can solve the problems of different fabric properties and other changes
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Embodiment 1
[0051] CH of anhydrous tert-butanol (0.5mol, 68.66g) 2 Cl 2 (50mL) solution was added dropwise under ice bath conditions (0°C-5°C) in CH 2 Cl 2 (100mL) solution, the dropwise addition is completed, after continuing the reaction at 0°C--5°C for 1h, add trifluoroethanol (1mol, 100.04g) dropwise in CH 2 Cl 2 (50 mL) solution. After completion of the dropwise addition, warm up to room temperature and react overnight (12h), heat to reflux for 3h and distill under reduced pressure to collect the fraction at 62°C / 10mmHg, which is difluoroalkoxyphosphonic acid. Gas-mass spectrometer, data analysis and characterization are as follows:
[0052] 1 HNMR (400MHz, CDCl3 ) : δ4.46(m, 4H), 7.04(d, J=755.6, H).
[0053] 19 F NMR (376MHz, CDCl 3 ): δ-74.8(m, 6F).
[0054] GC-MS m / z (EI, 70ev): 247[M+1]. +
[0055] IR (thin film, cm -1 ): 1460, 1420, 1285, 1175, 1110, 993, 845.
Embodiment 2
[0057] A solution of bisfluoroalkoxyphosphonic acid (117.9 g, 0.48 mol) in anhydrous acetonitrile (80 mL) was added at one time to trichloroisocyanuric acid (37.2 g, 0.16 mol) in anhydrous acetonitrile (240 mL), and the reaction solution Stir at room temperature for about 10 minutes, after a white precipitate appears, stir for another 5 minutes, filter the reaction solution, remove the solvent, and collect fractions at 62°C / 10mmHg by distillation under reduced pressure. Colorless fuming liquid bisfluorinated alkoxyphosphonyl chloride 1 HNMR (400MHz, CDCl 3 ): δ4.56-4.51(m, 4H).
[0058] 19 F NMR (376MHz, CDCl 3 ): δ-74.2 (6F, J=8.6Hz, t).
[0059] GC-MS m / z (EI, 70ev): 281[M+1] + .
[0060] IR (thin film, cm -1 ): 1458, 1420, 1300, 1175, 1080, 970, 890, 848.
Embodiment 3
[0062] CH 2 Cl 2 (30mL) solution was added dropwise to CH 2 Cl 2 (20mL) solution, after the dropwise addition, keep at 0°C for 3h, rise to room temperature for 12h, add ethyl acetate to dilute and extract the reaction, wash the reaction solution with an appropriate amount of water to remove unreacted hydroxyethylacrylamide and The triethylamine hydrochloride that generates is washed with an appropriate amount of saturated aqueous sodium chloride solution, dried over magnesium sulfate, filtered, and spin-dried to obtain the acrylamide monomer (7.1g , yield 81%).
[0063] 1 HNMR (400MHz, CDCl 3 ): δ3.65-3.69 (m, 2H), 4.25-4.31 (m, 2H), 4.39-4.48 (m, 4H), 5.70 (dd, J=1.6Hz, 10.4Hz, 1H), 6.19 (dd, J=10.4Hz, 17.4Hz, 1H), 6.32(dd, J=1.6Hz, 17.4Hz, 1H), 6.88(s, 1H).
[0064] 19 F NMR (376MHz, CDCl 3 ): δ75.62 (t, J=8.65Hz, 6F)
[0065] GC-MS m / z (EI, 70ev): 345 [M-CH 2 ] + , 324[M-CH 2 -F] + , 305[M-C 3 h 3 O] + ,
[0066] 275[M-CH 2 -CF 3 ] + , 245[M-CH 2 -OCH ...
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