A kind of preparation method of hexaphenoxycyclotriphosphazene flame retardant
A technology for hexaphenoxy cyclotriphosphazene and hexachlorocyclotriphosphazene, which is applied in the field of phosphorus-nitrogen compound synthesis, can solve the problems of troublesome separation and purification, complicated operation, slow reaction speed and the like, and achieves simplified separation and purification methods and steps , the preparation process is simple, and the effect of avoiding cost waste
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Embodiment 1
[0025] In a 500ml flask, add 17.2g sodium hydroxide, 35.5g phenol, 1g potassium iodide, add to 200g acetone, react for 2 hours, then add 18g hexachlorocyclotriphosphazene into the system, reflux when the system heats up, and react at 90°C for 10 Hours, cooling and filtering, the filtrate crystallized at -18 ° C, the resulting solid was washed with 100 ° C 5% sodium hydroxide aqueous solution for 3 hours, then filtered at room temperature to obtain 34.4 g of the product white powdery solid, the yield was 95.3%, and the purity was 97.2% .
Embodiment 2
[0027] In a 500ml flask, add 17.2g sodium hydroxide, 35.5g phenol, 0.5g potassium chloride, add in 200g acetonitrile, react for 1 hour, then add 18g hexachlorocyclotriphosphazene in the system, reflux when the system heats up, 80 ℃ for 6 hours, cooling and filtering, the filtrate crystallized at -18 ℃, the obtained solid was washed with 100 ℃ 4% sodium hydroxide aqueous solution for 3 hours, and then filtered at room temperature to obtain 34.9 g of the product white powdery solid, with a yield of 96.7%. Purity 97.0%.
Embodiment 3
[0029] In a 500ml flask, add 17.2g sodium hydroxide, 35.5g phenol, 0.8g potassium iodide, add 200g DMF, react for 2 hours, then add 18g hexachlorocyclotriphosphazene into the system, reflux when the system heats up, and react at 83°C After 3 hours, the temperature was lowered and filtered, and the filtrate was crystallized at -18 ° C. The obtained solid was washed with 100 ° C 3% sodium hydroxide aqueous solution for 5 hours, and then filtered at room temperature to obtain 34.6 g of the product white powdery solid, with a yield of 96.1% and a purity of 98.1 %.
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