Synthesis method and application of a phosphorus-containing and silicon-containing organic-inorganic internal hybrid active monomer
A technology of active monomers and synthetic methods, which is applied in organic chemistry, chemical instruments and methods, compounds of Group 5/15 elements of the periodic table, etc., can solve the problems that the ratio of elements cannot be controlled more precisely and the method is complicated , to achieve precise and controllable element composition, simple synthesis method, and improved heat resistance
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Embodiment 1
[0021] Add 11.68mL KH550 (50mmol), 6.7g 4-hydroxyphenyl formaldehyde (55mmol), 11.9g DOPO (55mmol) and 300mL chloroform into a 1000mL round bottom flask connected with a condenser, and stir the reaction at 50°C for 12h. After the reaction was completed, the reaction solution was concentrated to about 50 mL by rotary evaporation, and then slowly dropped into iced methanol for precipitation. It was filtered under reduced pressure, washed three times with methanol, and freeze-dried to obtain a white solid.
[0022] Add 27.1g (0.05mol) of previously synthesized phenolic intermediate compound, 10.1g (0.10mol) of triethylamine and 100mL of dichloromethane to a 250mL single-necked round-bottomed flask in sequence, place it at 5°C, and slowly 10.5 g (0.10 mol) of methacryloyl chloride was added dropwise, and stirring was continued for 8 hours after the dropwise addition was completed. After the reaction was completed, triethylamine hydrochloride was removed by filtration, and washed ...
Embodiment 2
[0024] Add 11.68mL KH550 (50mmol), 4.9g 4-hydroxyphenyl formaldehyde (40mmol), 11.9g DOPO (55mmol) and 300mL chloroform into a 1000mL round bottom flask connected with a condenser, and stir the reaction at 50°C for 12h. After the reaction was completed, the reaction solution was concentrated to about 50 mL by rotary evaporation, and then slowly dropped into iced methanol for precipitation. It was filtered under reduced pressure, washed three times with methanol, and freeze-dried to obtain a white solid.
[0025] Add 27.1g (0.05mol) of previously synthesized phenolic intermediate compound, 10.1g (0.10mol) of triethylamine and 100mL of dichloromethane to a 250mL single-necked round-bottomed flask in sequence, place it at 5°C, and slowly 10.5 g (0.10 mol) of methacryloyl chloride was added dropwise, and stirring was continued for 8 hours after the dropwise addition was completed. After the reaction was completed, triethylamine hydrochloride was removed by filtration, and washed ...
Embodiment 3
[0027] 11.68mL KH550 (50mmol), 4.9g 4-hydroxyphenyl formaldehyde (40mmol), 11.9g DOPO (55mmol) and 300mL ethanol were added to a 1000mL round bottom flask connected with a condenser, and the reaction was stirred at 50°C for 12h. After the reaction was completed, the reaction solution was concentrated to about 50 mL by rotary evaporation, and then slowly dropped into iced methanol for precipitation. It was filtered under reduced pressure, washed three times with methanol, and freeze-dried to obtain a white solid.
[0028] Add 27.1g (0.05mol) of previously synthesized phenolic intermediate compound, 10.1g (0.10mol) of triethylamine and 100mL of dichloromethane to a 250mL single-necked round-bottomed flask in sequence, place it at 5°C, and slowly 10.5 g (0.10 mol) of methacryloyl chloride was added dropwise, and stirring was continued for 8 hours after the dropwise addition was completed. After the reaction was completed, triethylamine hydrochloride was removed by filtration, an...
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