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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975811Generated: November 4, 2026

Bisphenol A → Carbonic acid;4-[2-(4-hydroxyphenyl)propan-2-yl]phenol

https://huagongshe.com/reaction/1975811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBisphenol AHCID 6623—
ReactantPhenyl benzoateHCID 7169—
ReactantDiphenyl carbonateHCID 7597—
ReactantBioxyanionHCID 11081419—
ProductCarbonic acid;4-[2-(4-hydroxyphenyl)propan-2-yl]phenolHCID 15998799%

Reaction Conditions

Temperature160 °C

Reaction Steps

0.20 mol bisphenol A, 0.21 mol diphenyl carbonate, 3×10-6 mol tetrabutyl ammonium bibenzoate and 4×10-3 mol phenyl benzoate are taken in a 250 ml glass reactor equipped with stirrer, nitrogen inlet and distillation assembly. Under the blanket of nitrogen the contents in the reactor were heated by means of thermostatically controlled furnace to 160° C. for 11/2 hr. Subsequently, the temperature was increased to 230° C. and pressure reduced from atmospheric to 100 mm Hg, and on keeping constant the temperature and pressure for one hour, about 80% phenol was collected. Maintaining the temperature at 230° C., the pressure was decreased sequentially in a following way: 80 mm, 1/2 hour; 60 mm, 1/2 hour; 40 mm, 1/2 hour; 20 mm, 1/2 hour; 10 mm, 1/2 hour and 1 mm, 1/2 hour. It was then observed that phenol removal was almost quantitative. Finally reaction mixture was heated to 280° C. at 1 mm for one hour to remove any residual phenol. The polymer, bisphenol A polycarbonate obtained in 99% yield was colorfree and its relative viscosity measured in chloroform at 25° C. in an ubbelohde viscometer was 1.26.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05288838
Source datasetuspto-grants-1994_02
ORD IDord-6cdaa9d93b854f038e1ad895bd887e79
Source noteuspto-grants-1994_02