The preparation method of phenyl dimethoxy (phosphacyclomethoxy) silane compound
A technology of flame retardant phenyl dimethoxy and silane compounds, which is applied in the field of preparation of flame retardant phenyl dimethoxy silane compounds, can solve problems such as threats to life safety, poor electrical performance, and use restrictions, and achieve High decomposition temperature, promotion of flame retardant effect, and effect of preventing melt dripping
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Embodiment 1
[0024] Example 1 In a 200ml four-neck flask equipped with a stirrer, a thermometer, and a high-efficiency fractionation device, replace the air in the bottle with nitrogen, and add 19.40g (0.10mol) of 4-hydroxymethyl-4-ethyl-cycloformazol Base phosphonate, 19.83g (0.10mol) phenyltrimethoxysilane, 40ml diethylene glycol dimethyl ether, heat up to 140°C, control the fractionation column top temperature not higher than 65°C, fractionate the generated methanol, and react 5h, after no methanol is produced, change it to a vacuum distillation device, diethylene glycol dimethyl ether (recovered and used) is removed by vacuum distillation, then add 35ml of toluene, stir, transfer to a separatory funnel to stand for stratification, The lower layer material liquid was separated, and a small amount of toluene and low boiling point substances were removed by distillation under reduced pressure to obtain light yellow liquid phenyldimethoxy (phosphacyclomethoxy) silane with a product yield of...
Embodiment 2
[0025] Example 2 In a 200ml four-neck flask equipped with a stirrer, a thermometer, and a high-efficiency fractionation device, replace the air in the bottle with nitrogen, and add 19.40g (0.10mol) of 4-hydroxymethyl-4-ethyl-cycloformazol Base phosphonate, 25.78g (0.13mol) phenyltrimethoxysilane, 50ml ethylene glycol diethyl ether, raise the temperature to 120°C, control the temperature at the top of the fractionation column to not be higher than 65°C, fractionate the generated methanol, and react for 7h. After no methanol is produced, change it to a vacuum distillation device, and remove ethylene glycol diethyl ether (recovery and use) by vacuum distillation, then add 70ml of toluene, stir, transfer to a separatory funnel to stand for stratification, and separate the lower layer of material Liquid, a small amount of toluene and low boiling point substances were distilled off under reduced pressure to obtain light yellow liquid phenyl dimethoxy (phosphacyclomethoxy) silane, and...
Embodiment 3
[0026] Example 3 In a 200ml four-neck flask equipped with a stirrer, a thermometer, and a high-efficiency fractionation device, replace the air in the bottle with nitrogen, and add 19.40g (0.10mol) of 4-hydroxymethyl-4-ethyl-cycloformazol Base phosphonate, 27.76g (0.14mol) phenyltrimethoxysilane, 80ml DMF, raise the temperature to 130°C, control the temperature at the top of the fractionation column to not be higher than 65°C, fractionate the generated methanol, fractionate for 6h, and wait for no methanol After producing, change into vacuum distillation device, vacuum distillation removes DMF (recovery use), then add the toluene of 50ml, stir, transfer to the separating funnel and leave standstill layering, separate lower layer material liquid, vacuum distillation removes a small amount of Toluene and low-boilers yielded a pale yellow liquid phenyl dimethoxy (phosphacyclomethoxy) silane with a yield of 96.8%.
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