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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51173Generated: October 24, 2026

Phenol → BPA phosphate

https://huagongshe.com/en/reaction/51173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantBisphenol AHCID 6623—
ReactantPhosphorodichloridic acid, phenyl esterHCID 13038—
ReactantPotassium HydroxideHCID 14797—
ReactantAluminum(III) ChlorideHCID 6451240—
ProductBPA phosphateHCID 8659130991%

Reaction Conditions

Temperature120 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713598B2
Source datasetuspto-grants-2004_03
ORD IDord-eb27ec21563845408defb3a914903282
Source noteuspto-grants-2004_03