反応 #834825

反応方程式

Chloroethyl vinyl ether

4-Hydroxy-3,5-dimethylphenyldiphenylsulfonium perfluorobutanesulfonate salt

potassium carbonate

N,N,N′,N′-tetramethylethylenediamine

→

4-vinyloxyethoxy-3,5-dimethylphenyldiphenylsulfonium perfluorobutanesulfonate salt

溶媒

dimethyl sulfoxide

反応条件

後処理

1. 1
   温度cooled to 30° C.
2. 2
   その他After removal of solid
3. 3
   ろ過through filtration, water (280 g)
4. 4
   workup.ADDITIONwas added to the filtrate
5. 5
   洗浄the aqueous layer was washed three times with hexane (168 g)
6. 6
   workup.ADDITIONTo the washed aqueous layer, dichloromethane (226 g) and water (50 g) were added
7. 7
   workup.STIRRINGunder stirring
8. 8
   抽出whereby the target substance was extracted to the dichloromethane layer
9. 9
   洗浄The organic layer was repeatedly washed with distilled water until the pH of the separated aqueous layer
10. 10
    その他The solvent was removed by means of a rotary evaporator

実験手順

4-Hydroxy-3,5-dimethylphenyldiphenylsulfonium perfluorobutanesulfonate salt (56.1 g), potassium carbonate (18.4 g), and N,N,N′,N′-tetramethylethylenediamine (1.07 g) were dissolved in dimethyl sulfoxide (118 g). Chloroethyl vinyl ether (14.2 g) was added to the solution, followed by heating to 80° C. The reaction mixture was stirred for 47 hours and cooled to 30° C. or lower. After removal of solid through filtration, water (280 g) was added to the filtrate, and the aqueous layer was washed three times with hexane (168 g). To the washed aqueous layer, dichloromethane (226 g) and water (50 g) were added under stirring, whereby the target substance was extracted to the dichloromethane layer. The organic layer was repeatedly washed with distilled water until the pH of the separated aqueous layer was shifted to 7. The solvent was removed by means of a rotary evaporator, to thereby yield 41.0 g of an oily substance. Through 1H-NMR and ion chromatography, the substance was identified to be 4-vinyloxyethoxy-3,5-dimethylphenyldiphenylsulfonium perfluorobutanesulfonate salt.

出典