Organic phosphate rare earth salt nucleater, synthesis method and application thereof
An organic phosphate ester and synthesis method technology, which is applied in the fields of fine chemicals and polymer materials, can solve the problems of insignificant anti-reflection effect and high melting point, and achieve the effect of effective and feasible process, wide practicability and wide applicability
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Embodiment 1
[0040] Embodiment 1: the synthesis of two (2,4-dimethylphenoxy) lanthanum phosphates
[0041] Add the ethanol solution that contains 306g two (2,4-dimethylphenoxy) phosphoric acid in reactor, its structural formula is as shown in general formula (IV), R 1 , R 2 For methyl. Under stirring, 20% sodium hydroxide aqueous solution containing 64 g of sodium hydroxide was added, and it was made to react at 80 degreeC for 2 hours. Then, a 20% aqueous solution of lanthanum chloride containing 343.7 g of lanthanum chloride was added, followed by stirring at normal temperature for 2 hours. After the reaction, filter, dry, and pulverize to obtain 440.3 g of bis(2,4-dimethylphenoxy)lanthanum phosphate.
Embodiment 2
[0042] Embodiment 2: the synthesis of 2,2'-methylene-bis(4,6-dimethylphenoxy)lanthanum phosphate
[0043] In reactor, add the ethanol solution that contains 318g 2,2'-methylene-bis(4,6-dimethylphenoxy)phosphoric acid, its structural formula is as shown in general formula (III), R 1 , R 2 For methyl. Under stirring, 20% sodium hydroxide aqueous solution containing 64 g of sodium hydroxide was added, and it was made to react at 100 degreeC for 1 hour. Then, a 15% aqueous solution of lanthanum chloride containing 368.25 g of lanthanum chloride was added, followed by stirring at 80° C. for 1 hour. After completion of the reaction, filter, dry, and pulverize to obtain 447.93 g of 2,2'-methylene-bis(4,6-dimethylphenoxy)lanthanum phosphate.
Embodiment 3
[0044] Embodiment 3: two (2, the synthesis of 4-di-tert-butylphenoxy) cerium phosphate
[0045] Add the methanol solution that contains 474g two (2,4-di-tert-butylphenoxy) phosphoric acid in the reactor, its structural formula is as shown in general formula (IV), R 1 , R 2 For tert-butyl. Under stirring, 20% sodium hydroxide aqueous solution containing 56 g of sodium hydroxide was added, and it reacted at 80 degreeC for 2 hours. Then, 20% cerium chloride aqueous solution containing 394.8g of cerium chloride was added, and it stirred at normal temperature for 2 hours. After the reaction, filter, dry, and pulverize to obtain 620.78 g of bis(2,4-di-tert-butylphenoxy)cerium phosphate.
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