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HRID 51172作成日:2026年10月23日

Phenol → BPA phosphate

https://huagongshe.com/ja/reaction/51172

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物Bisphenol AHCID 6623—
反応物Phosphorodichloridic acid, phenyl esterHCID 13038—
反応物Potassium HydroxideHCID 14797—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物BPA phosphateHCID 86591309—

反応条件

温度120 °C

反応手順

97.49 g (0.43 mol) of BPA, 100.00 g (0.47 mol) of phenyldichlorophosphate, and 0.89 g (6.66 mmol) of aluminum chloride were taken in a reaction kettle. The kettle was fitted with an overhead stirrer, a water condenser with nitrogen outlet and a nitrogen inlet. The nitrogen outlet was immersed in a beaker containing KOH solution to absorb the evolved HCl. The reaction mixture was stirred-at 90° C. for 2 h and further at 120° C. for 4 h. A sample of the reaction mixture was drawn and 31P NMR was done to show that there was no phenyldichlorophosphate left and the conversion was nearly 75%. To the reaction mixture 26.06 g (0.28 mol) of phenol was added and the temperature was increased to 140° C. and the reaction mixture was stirred at that temperature for 3 h. After confirming from the 31P NMR spectrum that there was no reactive P—Cl bonds, the reaction mixture was cooled down to room temperature and dissolved in minimum amount of methylene chloride. The methylene chloride solution was added slowly into an excess amount of methanol. The methanol solution was decanted and the precipitate was again dissolved in a minimum amount of methylene chloride and poured into excess methanol. After decanting the methanol solution the precipitate was dried in a vacuum oven at 60-80° C. for 6 h to give 135 g (yield, ˜87%) of the desired solid poly(BPA-phosphate).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713598B2
出典データセットuspto-grants-2004_03
ORD IDord-4d24c050fa76405b92ea9ef4809f20d5
出典メモuspto-grants-2004_03