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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27724Generated: October 25, 2026

Isophthalic Acid → Bisphenol A

https://huagongshe.com/reaction/27724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsophthalic AcidHCID 8496—
ReactantPotassium HydroxideHCID 14797—
ReactantPhenol, 4,4'-(1-methylethylidene)bis-, 1,1'-diacetateHCID 82437—
ReactantHCID 18669760HCID 18669760—
Reactant2,6-Dimethylphenol chloroform ethanolHCID 131711879—
ProductBisphenol AHCID 6623—

Reaction Conditions

Temperature290 °C

Reaction Steps

An equimolar mixture of 2,2-bis(4-acetoxyphenyl)propane (Bisphenol A diacetate) and isophthalic acid is heated gradualy to 290° C. in a stirred vessel under gradually increasing vacuum to remove the acetic acid which is liberated. When the melt viscosity of the condensate reaches a level such that stirring becomes difficult the melt is drained from the reaction vessel and crystallized. The crystallized polymer is subjected to solid state polymerization under vacuum at 280° C. until the inherent viscosity reaches 0.65 dl/g (in 40/60 by weight tetrachloroethane/phenol solution at 25° C.). The polymer is then extruded at 350° C. and pelletized. The polymer has an inherent viscosity of 0.62 and a carboxylic acid content of 40 microequivalents per gram (μeq./g), determined by potentiometric titration of a solution of the polymer in a 2,6-dimethylphenol/chloroform/ethanol mixture with an ethanolic solution of potassium hydroxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04222932
Source datasetuspto-grants-1980_09
ORD IDord-da044c87e1ee442cbdf8d9c420ead15b
Source noteuspto-grants-1980_09