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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295333Generated: October 31, 2026

Acetone → Bisphenol A

https://huagongshe.com/reaction/2295333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPhenolHCID 996—
ReactantSodium HydroxideHCID 14798—
ReactantSodium sulfide nonahydrateHCID 73972—
Reactant1-Propanethiol, 3-amino-HCID 97436—
ReactantHomocystamineHCID 193295—
ReactantSulfurHCID 5362487—
ReactantHCID 178514650HCID 178514650—
ProductBisphenol AHCID 6623—

Reaction Steps

There was added to the above reaction mixture of the disulfide derivative of sulfonated polystyrene at a temperature of 50° C., 10 ml of a 50% sodium hydroxide solution and 20 grams of sodium sulfide nonahydrate. The resulting heterogeneous mixture was heated at reflux for 3.5 hours. The cooled reation mixture was filtered and the resin was washed with water followed by 1 liter of a 10% sulfuric acid solution. The resulting washed resin was then azeotropically dried with toluene. Based on method of preparation, there was obtained an ion-exchange catalyst consisting of about 20 mole percent of chemically combined sulfonated styrene units having aminopropylmercaptan units covalently attached to sulfur by nitrogen-sulfur linkages and about 80 mole percent of sulfonated styrene units. This ion-exchange resin was found to be an effective condensation catalyst for phenol and acetone to provide for the production of bisphenol-A in accordance with the procedure of Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04424283
Source datasetuspto-grants-1984_01
ORD IDord-e68b436d629e419b8a593c101c250ee2
Source noteuspto-grants-1984_01