Reacción #834826
ord-0ef5d57c90774179a9adb9b108e1ffed
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturacooled to 30° C.
- 2OtroAfter removal of solid
- 3Filtraciónthrough filtration, water (220 g) and dichloromethane (113 g)
- 4workup.ADDITIONwere added to the filtrate, whereby the target substance
- 5Extracciónwas extracted to the dichloromethane layer
- 6LavadoThe organic layer was repeatedly washed with distilled water until the pH of the separated aqueous layer
- 7OtroThe solvent was removed by means of a rotary evaporator
- 8workup.DISSOLUTIONthe formed oily substance was dissolved in acetonitrile (100 g)
- 9LavadoThe acetonitrile layer was washed five times with hexane (85 g)
- 10OtroThe solvent was removed by means of a rotary evaporator
Procedimiento
4-Hydroxyphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt (28.4 g), potassium carbonate (8.56 g), and N,N,N′,N′-tetramethylethylenediamine (0.50 g) were dissolved in dimethyl sulfoxide (143 g). Chloroethyl vinyl ether (6.30 g) was added to the solution, followed by heating to 80° C. The reaction mixture was stirred for 15 hours and cooled to 30° C. or lower. After removal of solid through filtration, water (220 g) and dichloromethane (113 g) were added to the filtrate, 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, and the formed oily substance was dissolved in acetonitrile (100 g). The acetonitrile layer was washed five times with hexane (85 g). The solvent was removed by means of a rotary evaporator, to thereby yield 24.5 g of a brown oily substance. Through 1H-NMR and ion chromatography, the substance was identified to be 4-vinyloxyethoxyphenyldi(4-t-butylphenyl)sulfonium perfluorobutanesulfonate salt.