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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 30945생성일: 2026년 10월 24일

Phosgene → bisphenol A 4,4'-dihydroxydiphenyl ether

https://huagongshe.com/ko/reaction/30945

반응식

참여 물질

역할이름HCID투입량
반응물PhosgeneHCID 6371—
반응물Bisphenol AHCID 6623—
반응물4-tert-ButylphenolHCID 7393—
반응물N-EthylpiperidineHCID 13007—
반응물Sodium HydroxideHCID 14798—
반응물4,4'-Dihydroxydiphenyl etherHCID 16069—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물bisphenol A 4,4'-dihydroxydiphenyl etherHCID 131727054—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425358B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-0adbd292420248bea1ac156233c46655
출처 메모uspto-grants-2008_09