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HRID 30952作成日:2026年10月24日

Phosgene → bisphenol A 4,4'-dihydroxydiphenyl ether

https://huagongshe.com/ja/reaction/30952

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

31 litres of methylene chloride are added to a solution, rendered inert with nitrogen, of 3903.9 g (17.1 mol.) of bisphenol A, 182 g (0.9 mol.) of 4,4′-dihydroxydiphenyl ether and 1584 g (39.6 mol.) of sodium hydroxide in 31 litres of water. In a one-step procedure, 108.14 g (0.72 mol. or 4 mol. % relative to bisphenol A) of p-tert.-butylphenol (BUP) are added as chain terminator. At a pH value of 13.4 and at 21° C., 3560 g (36 mol.) of phosgene are added in the course of 1 hour and 20 minutes. In order to prevent the pH value from falling below 12.6, 25% sodium hydroxide solution was added during the phosgenation. When the phosgenation is complete, and after rinsing with nitrogen, 24.7 ml (0.18 mol., 1 mol. % relative to bisphenol A) of n-ethylpiperidine are 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. After replacing the solvent with chlorobenzene, the product is extruded at 290° C. using an evaporating extruder.

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-bb40376617ed4778a10a74eb95eecb2b
出典メモuspto-grants-2008_09