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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112367Generated: October 25, 2026

Phenol → Bisphenol A

https://huagongshe.com/reaction/2112367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantResorcinolHCID 5054—
ReactantPhosgeneHCID 6371—
ReactantSodium HydroxideHCID 14798—
ReactantTributylmethylammoniumHCID 36209—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductBisphenol AHCID 6623—

Reaction Steps

Into a 500 ml Morton flask equipped with a mechanical stirrer, a reflux condenser, a nitrogen bypass, a pH probe and a phosgene dip tube was placed 6.88 g of resorcinol, 100 ml of methylene chloride, 20 ml of water and 0.5 ml of 75 wt % aqueous methyltributylammonium (MTBA). The pH was adjusted to and maintained at 7 with 25 wt % of NaOH as 29 g of a 35 wt % solution of diacid chlorides (DACS) in methylene chloride (delivers 50 mmol of 50/50 isophthaloyl chloride (IPC)/terephthaloyl chloride (TPC)) was added over 4 minutes. The pH was raised to 10 and 100 μl of triethylamine (TEA), 50 mg of water and 0.21 g of phenol were added. The pH was maintained at 10 and 4.0 g of phosgene was added at 0.5 g/min. The final pH was 10.1. The polymer solution was separated from the brine by centrifugation and washed 1 time with 1N HCl and 3 times with deionized water. The polymer was isolated by hot water crumbing in a blender and collected by filtration and washed with water and dried in a vacuum oven at 110° C. overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524562B2
Source datasetuspto-grants-2009_04
ORD IDord-fc1d59adaf3240b586343ea1f382c981
Source noteuspto-grants-2009_04