Reacción #582512

Ecuación de reacción

2,2′-azobis(2,4-dimethylvaleronitrile)

styrene

4-vinylbenzenesulfonic acid cyclohexyl ester

2,2′-azobis(2,4-dimethylvaleronitrile)

→

styrene 4-vinylbenzenesulfonic acid cyclohexyl ester

Disolventes

methyl ethyl ketone

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroA three-necked flask having
2. 2
   workup.ADDITIONwas dropwise added
3. 3
   workup.ADDITIONwas further added
4. 4
   workup.STIRRINGby stirring for further 2 hours

Procedimiento

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.

Fuente