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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32926Generated: October 29, 2026

Phenol → BPA phenol

https://huagongshe.com/reaction/32926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantBisphenol AHCID 6623—
SolventWaterHCID 962—
ProductBPA phenolHCID 14618994—

Reaction Steps

A process for the preparation of high purity bisphenol A is disclosed. The multi-step process entails a) reacting phenol with acetone in the presence of an acidic ion exchanger and a sulfur-containing co-catalyst to give a product mixture that includes bisphenol A and phenol; b) continuously obtaining from the product mixture crystals of bisphenol A-phenol adduct by suspension crystallization, c) separating the adduct obtained in step (b) by solid-liquid separation to obtain a solid phase and a liquid phase d) washing of the solid phase with a solution containing phenol to obtain washed solid phase and a second liquid phase, e) distilling the liquid phase and said second liquid phase to obtain dewatered solution containing 5 to 15% p,p-BPA, 3 to 12% isomers of BPA and less than 0.3% water, f) introducing of at least 90% by weight of the dewatered solution into step (a), g) adding phenol to the washed solid phase obtained in step d) to obtain a homogeneous material system that contains p,p′-BPA, isomers of BPA and water h) continuously obtaining from the homogeneous material system crystals of bisphenol A-phenol adduct by suspension crystallization; i) separating the crystals obtained in step (h) by solid-liquid separation to obtain a second solid phase, j) washing the second solid phase with a solution that contains phenol to obtain a washed adduct; and k) heating the washed adduct to remove phenol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427694B2
Source datasetuspto-grants-2008_09
ORD IDord-3dbe239ce42d485b840f345a6a496bc1
Source noteuspto-grants-2008_09