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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888559Generated: October 31, 2026

Phosgene → 4-(2-(4-Hydroxyphenyl)propan-2-yl)-2-methoxyphenol

https://huagongshe.com/reaction/888559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantBisphenol AHCID 6623—
Reactant4-CumylphenolHCID 11742—
ReactantSodium GluconateHCID 23672301—
ReactantHCID 86642583HCID 86642583—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
Product4-(2-(4-Hydroxyphenyl)propan-2-yl)-2-methoxyphenolHCID 23517248—

Reaction Steps

Run 3—1% guaiacol BPA: Methylene chloride (23 L), water (8 L), BPA (4500 g, 19.8 mol), monomethoxyBPA (55 g of the above mixture), p-cumylphenol (135 g, 0.64 mol), triethylamine (40 ml) and sodium gluconate (10 g) was charged to a 75 L reactor equipped with mechanical agitation, condenser, and caustic scrubber vent system. Phosgene (2300 g, 23.2 mol) was added at a rate of 80 g/min to the reactor while 33 wt % caustic was added at a rate to maintain pH=10. The reactor contents were purged with nitrogen then transferred to another tank and centrifuged to remove the brine layer. The organic layer containing the polymer was washed on a centrifuge train with 1N HCl and then with deionized water until residual chloride levels were <5 ppm. The polymer was isolated by steam precipitation followed by drying under hot nitrogen. The final dried resin weighed 4.1 lbs, had Mw=27652 daltons and PDI=2.5 by GPC vs PC standard, <1 ppm TEA, 0.6 ppm chloride ion, <10 ppm residual free BPA, and <0.05 ppm Fe. The glass transition temperature was determined to be 153 C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247619B2
Source datasetuspto-grants-2012_08
ORD IDord-9cd320e369464a4198773a66d9bd6090
Source noteuspto-grants-2012_08