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HRID 495332作成日:2026年10月25日

Styrene → Styrene 4-vinylbenzenesulfonic acid cyclohexyl ester

https://huagongshe.com/reaction/495332

反応式

関与物質

役割名称HCID仕込み量
反応物StyreneHCID 7501—
反応物4-Styrenesulfonic acidHCID 75905—
反応物2,2'-Azobis(2,4-dimethylvaleronitrile)HCID 91537—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物Styrene 4-vinylbenzenesulfonic acid cyclohexyl esterHCID 86585263—

反応条件

温度65 °C

反応手順

A three-necked flask having a capacity of 500 ml was charged with 240 g of methyl ethyl ketone and the content was stirred at 65° C in a nitrogen gas stream. A mixture of 93.74 of styrene, 26.64 g of 4-vinylbenzenesulfonic acid cyclohe ester and 1.99 g of 2,2′-azobis(2,4-dimethylvaleronitrile) was dropwise added thereto over 2 hours. After completion of the dropwise addition, 0.5 g of 2,2′-azobis(2,4-dimethylvaleronitrile) was further added, followed by stirring for further 2 hours, thereby a styrene-4-vinylbenzenesulfonic acid cyclohexyl ester copolymer was obtained. After the reaction mixture was poured into an egg-plant type flask having a capacity of 1 liter and concentrated, 300 g of MFG was added thereto, the reaction mixture was heated for 3 hours with refluxing MFG, thereby sulfonic acid cyclohexyl ester was decomposed to obtain a sulfonic acid. The obtained reaction mixture was cooled to room temperature and poured into a beaker containing 3 liters of water, thus an aqueous solution of a high molecular compound was prepared.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06939658B2
出典データセットuspto-grants-2005_09
ORD IDord-a4431b8c7f824b30b04ac3d80b1f5c6c
出典メモuspto-grants-2005_09