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HRID 743414作成日:2026年10月27日

Dithionite → Bisphenol A

https://huagongshe.com/reaction/743414

反応式

関与物質

役割名称HCID仕込み量
反応物DithioniteHCID 1086—
反応物PhosgeneHCID 6371—
反応物4-tert-ButylphenolHCID 7393—
反応物Sodium HydroxideHCID 14798—
反応物bisphenol AFHCID 73864—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物Bisphenol AHCID 6623—

反応手順

2371 Parts of deionized water, 156 parts of a 48.5% aqueous sodium hydroxide solution, and 0.6 parts of hydrosulfite were placed in-the same apparatus as used in Example 1, and after deoxidation was carried out in the same way as in Example 1, 157.6 parts of bisphenol AF of 99.98% purity and 134.6 parts of bisphenol FL of 99.8% purity were dissolved therein, then 2548 parts of methylene chloride was added, and 98.5 parts of phosgene was blown thereinto at 13° to 16° C. over about 50 min with stirring. Then, 53.2 parts of a 48.5% aqueous sodium hydroxide solution and 8.5 parts of p-tert-butylphenol were added and after they were emulsified by stirring, 0.2 parts of triethylamine was added, followed by stirring at 30° C. for about 2 hours, to complete the reaction. Then the reaction mixture was treated in the same way as in Example 1, to obtain a copolymerized polymer. The specific viscosity of this copolymerized polymer was 0.178, the retention of the specific viscosity after the steam treatment was 85% and the glass transition temperature was 215° C., which show high hydrolysis resistance and high heat resistance, the light transmittance was 89%, which is good, the light transmittance after the heat treatment was 89%, showing excellent heat stability; and the oxidation resistance was remarkably excellent in comparison with the polymer obtained from bisphenol A as shown by curve 3 (.diamond.) in FIG. 2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05556904
出典データセットuspto-grants-1996_09
ORD IDord-fa4376941b8043da96949d32c4904a2d
出典メモuspto-grants-1996_09