Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353311Generated: October 30, 2026

Phenol → Bisphenol A

https://huagongshe.com/reaction/353311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantPhenol AcetoneHCID 54464289—
SolventAcetoneHCID 180—
ProductBisphenol AHCID 6623—

Reaction Steps

Phenol and acetone were passed through a column type reactor in which an ion exchange resin having a sulfonic group packed, in a molar ratio of phenol/acetone of 13, and a reaction solution of bisphenol A was obtained with 95% of conversion of acetone by a reaction at an inlet temperature of 55° C. and an outlet temperature of 75° C. Then, the above reaction solution was subjected to distillation to remove low boiling point substances such as unreacted acetone and water as a by-product, followed by crystallization at 50° C. by means of external intercooling to obtain a slurry containing an adduct crystal (adduct) comprising bisphenol A and phenol. The crystal adduct slurry was subjected to filtration under reduced pressure by means of a filter having a filter cloth with an aperture of 106 μm set thereto, while keeping the slurry temperature at 50° C., and the obtained crystal adduct cake was washed with refined phenol. The finally obtained adduct was a mixture with a composition of bisphenol A/phenol=7/3 (weight ratio). Impurities in the adduct at this stage were 2,4-bisphenol A=84 ppm, chroman-1=5 ppm and trisphenol=30 ppm, and no 4-isopropenyl phenol was detected. In order to hold the adduct in a molten state in a stock tank (made of SUS316) under conditions of the temperature and time as identified in Table 1, phenol was added to obtain a composition adjusted to have the composition as identified in Table 1. Then, the composition was held in a molten state under normal pressure under nitrogen sealing under conditions as identified in Table 1, and then the content of 4-isopropenyl phenol (IPP) contained in the composition was measured. The results are shown in Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06750314B2
Source datasetuspto-grants-2004_06
ORD IDord-f86d0d5e13174f648758edb4a6d84fbd
Source noteuspto-grants-2004_06