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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51172Generated: October 23, 2026

Phenol → BPA phosphate

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantBisphenol AHCID 6623—
ReactantPhosphorodichloridic acid, phenyl esterHCID 13038—
ReactantPotassium HydroxideHCID 14797—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductBPA phosphateHCID 86591309—

Reaction Conditions

Temperature120 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713598B2
Source datasetuspto-grants-2004_03
ORD IDord-4d24c050fa76405b92ea9ef4809f20d5
Source noteuspto-grants-2004_03