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HRID 30948作成日:2026年10月25日

Phosgene → bisphenol TMC 4,4'-dihydroxydiphenyl ether

https://huagongshe.com/reaction/30948

反応式

関与物質

役割名称HCID仕込み量
反応物PhosgeneHCID 6371—
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—
反応物4,4'-(3,3,5-Trimethylcyclohexylidene)bis(phenol)HCID 4134035—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物bisphenol TMC 4,4'-dihydroxydiphenyl etherHCID 131727055—

反応手順

130 ml of methylene chloride are added to a solution, rendered inert with nitrogen, of 7.077 g (0.035 mol.) of 4,4′-dihydroxydiphenyl ether and 10.87 g (0.035 mol.) of bisphenol TMC as well as 6.16 g (0.154 mol.) of sodium hydroxide in 130 ml of water. In a one-step procedure, 0.368 g (0.0024 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, 9.7 ml (13.8 g, 0.14 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, 0.10 ml (0.0007 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 14.08 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-7311ef6d8dd041a89e2326b3f0fb7878
出典メモuspto-grants-2008_09