反応 #582513

ord-7f56976afb524574b67fe6ae1edfd931

反応方程式

CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C
2,2′-azobis(2,4-dimethylvaleronitrile)
C=Cc1ccccc1
styrene
C=Cc1ccc(S(=O)(=O)OC2CCCCC2)cc1
4-vinylbenzenesulfonic acid cyclohexyl ester
CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C
2,2′-azobis(2,4-dimethylvaleronitrile)
C=Cc1ccc(S(=O)(=O)OC2CCCCC2)cc1.C=Cc1ccccc1
styrene 4-vinylbenzenesulfonic acid cyclohexyl ester

反応条件

温度
65°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他A three-necked flask having
  2. 2
    workup.ADDITIONwas further added
  3. 3
    workup.STIRRINGby stirring for further 2 hours

実験手順

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. g of styrene, 26.64 g of 4-vinylbenzenesulfonic acid cyclohexyl 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.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US06939658B2uspto-grants-2005_09