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HRID 30945作成日:2026年10月24日

Phosgene → bisphenol A 4,4'-dihydroxydiphenyl ether

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

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
反応物Bisphenol AHCID 6623—
反応物4-tert-ButylphenolHCID 7393—
反応物N-EthylpiperidineHCID 13007—
反応物Sodium HydroxideHCID 14798—
反応物4,4'-Dihydroxydiphenyl etherHCID 16069—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物bisphenol A 4,4'-dihydroxydiphenyl etherHCID 131727054—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07425358B2
出典データセットuspto-grants-2008_09
ORD IDord-0adbd292420248bea1ac156233c46655
出典メモuspto-grants-2008_09