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HRID 325057作成日:2026年10月25日

Phenol → alpha,alpha'-Dimethyl-alpha,alpha,alpha',alpha'-tetrakis(4-hydroxyphenyl)-p-xylene

https://huagongshe.com/reaction/325057

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物1,4-DiacetylbenzeneHCID 13888—
生成物alpha,alpha'-Dimethyl-alpha,alpha,alpha',alpha'-tetrakis(4-hydroxyphenyl)-p-xyleneHCID 22352143—

反応手順

0.0215 mols of α,α′-dimethyl-α,α,α′,α′-tetrakis(4-hydroxyphenyl)-p-xylene (produced from 1,4-diacetylbenzene and phenol and having a melting point of 307° C.), 9.2 mols of bisphenol A, 9.4 liters of an aqueous solution of 2.0 N sodium hydroxide, and 8 liters of dichloromethane were put into a 50 liters container equipped with a stirrer, and stirred therein, to which phosgene was introduced for 30 minutes. Next, 0.44 mols of bisphenol A, 0.022mols of triethylamine, and 4.5 liters of an aqueous solution of 0.2 N sodium hydroxide were added thereto, and reacted for 40 minutes, and thereafter the aqueous phase and the organic phase in the reaction mixture were separated from each other. Thus was prepared a dichloromethane solution of an oligocarbonate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06222004B1
出典データセットuspto-grants-2001_04
ORD IDord-af0f685bc8e84499939123ce07ee12b0
出典メモuspto-grants-2001_04