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HRID 743413作成日:2026年10月23日

Dithionite → Bisphenol A

https://huagongshe.com/ja/reaction/743413

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

1897 Parts of deionized water, 125 parts of a 48.5% aqueous sodium hydroxide solution, and 0.5 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, 183.5 parts of bisphenol AF of 99.98% purity and 47.9 parts of bisphenol FL of 99.8% purity were dissolved therein, then 2038 parts of methylene chloride was added, and 79.1 parts of phosgene was blown thereinto at 13° to 16° C. over about 50 min with stirring. Then, 42.5 parts of a 48.5% aqueous sodium hydroxide solution and 6.7 parts of p-tert-butylphenol were added and after they were emulsified by stirring, 0.17 part 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 0.177, the retention of the specific viscosity after the steam treatment was 80%, showing good hydrolysis resistance the glass transition temperature was 178° C. showing high heat resistance, the light transmittance was 89%, which is good, the light transmittance after the heat treatment was 80%, showing excellent heat stability, and the oxidation resistance was remarkably excellent in comparison with the polymer obtained from bisphenol A as shown by curve 2 (+) 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-e75a0520b96b4403970f933b254c68e7
出典メモuspto-grants-1996_09