참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenol | HCID 996 | — |
| 반응물 | Bisphenol A | HCID 6623 | — |
| 반응물 | Phosphorodichloridic acid, phenyl ester | HCID 13038 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | Aluminum(III) Chloride | HCID 6451240 | — |
| 생성물 | BPA phosphate | HCID 86591309 | 91% |
반응 단계
24.81 g (0.11 mol) of BPA, 25.00 g (0.12 mol) of phenyldichlorophosphate, and 0.22 g (1.64 mmol) of aluminum chloride were taken in a cylindrical glass reactor 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 hours and further at 120° C. for 4 hours. A sample of the reaction mixture was drawn and 31P NMR spectrum was done to show that there was no phenyidichlorophosphate left; the conversion was nearly 75%. To the reaction mixture 4.49 g (0.05 mol) of phenol was added and the temperature was increased to 140° C. and stirred at that temperature for 4 hours. After confirming from the 31P NMR spectrum that there were no reactive P—Cl bonds, vacuum (0.01 mm Hg) was applied at 120° C. for 2 hours to remove excess phenol. The temperature was further increased to 140° C. and then to a maximum for 180° C. and the reaction mixture was held under vacuum for additional 4 hours. The reaction mixture was poured while it was in molten state onto aluminum foil to afford 36 g (yield ˜91%) a straw yellow, transparent solid poly-(BPA-phosphate).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06713598B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-eb27ec21563845408defb3a914903282 |
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| 출처 메모 | uspto-grants-2004_03 |
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