Reacción #82545

Ecuación de reacción

1-fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene

tributyltin hydride

azobisisobutyronitrile

→

1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene

Disolventes

cyclohexane

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaat reflux for about three hours
2. 2
   workup.ADDITION125 mL of silica gel is added
3. 3
   ConcentraciónThe mixture is concentrated under reduced pressure
4. 4
   Concentraciónconcentrated under reduced pressure

Procedimiento

Under a nitrogen atmosphere, a stirring solution of 22.7 grams (0.067 mole) of 1-fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene, 42.0 grams (0.14 mole) of tributyltin hydride, and 0.5 gram (catalyst) of azobisisobutyronitrile in 700 mL of cyclohexane is heated at reflux for about three hours. After this time the reaction mixture is cooled to ambient temperature, and 125 mL of silica gel is added. The mixture is concentrated under reduced pressure, and the residue is subjected to column chromatography. The product-containing fractions are combined and concentrated under reduced pressure, yielding 1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene.

Fuente