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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30945Generated: October 26, 2026

Phosgene → bisphenol A 4,4'-dihydroxydiphenyl ether

https://huagongshe.com/reaction/30945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantBisphenol AHCID 6623—
Reactant4-tert-ButylphenolHCID 7393—
ReactantN-EthylpiperidineHCID 13007—
ReactantSodium HydroxideHCID 14798—
Reactant4,4'-Dihydroxydiphenyl etherHCID 16069—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Productbisphenol A 4,4'-dihydroxydiphenyl etherHCID 131727054—

Reaction Steps

126 ml of methylene chloride are added to a solution, rendered inert with nitrogen, of 8.088 g (0.04 mol.) of 4,4′-dihydroxydiphenyl ether and 9.132 g (0.04 mol.) of bisphenol A as well as 7.04 g (0.176 mol.) of sodium hydroxide in 126 ml of water. In a one-step procedure, 0.42 g (0.0028 mol. or 3.5 mol. % relative to bisphenol) of p-tert.-butylphenol (BUP) are added as chain terminator. At a pH value of 14 and at room temperature, 11 ml (15.8 g, 0.16 mol.) of phosgene are added in the course of 10 minutes. In order to prevent the pH value from falling below 12, 25% sodium hydroxide solution was added during the phosgenation. When the phosgenation is complete, and after rinsing with nitrogen, 0.11 ml (0.0008 mol., 1 mol. % relative to bisphenol) of n-ethylpiperidine is added as catalyst, and stirring is then carried out for one hour. The aqueous phase is separated off, and the organic phase is acidified with phosphoric acid and washed with distilled water until neutral and free of salt. Precipitation of the polymer in methanol and drying yield 5.76 g of polycarbonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07425358B2
Source datasetuspto-grants-2008_09
ORD IDord-0adbd292420248bea1ac156233c46655
Source noteuspto-grants-2008_09