Reacción #1951070

Ecuación de reacción

(4-Fluorophenyl) divinyl phosphine oxide

benzylamine

→

1-benzyl-4-(4-fluorophenyl)-[1,4]azaphosphinane 4-oxide

Rendimiento 82.0%

Disolventes

THF

water

Condiciones de reacción

Tratamiento posterior

1. 1
   ConcentraciónThe reaction mixture was concentrated by rotary evaporation
2. 2
   Extracciónthe product was extracted into dichloromethane
3. 3
   Lavadowashed with saturated brine
4. 4
   SecadoThe organic phase was dried with sodium sulfate
5. 5
   Filtraciónfiltered
6. 6
   Concentraciónconcentrated by rotary evaporation
7. 7
   Otroto yield 2.52 g of crude product
8. 8
   OtroImpurities were removed
9. 9
   LavadoThe product was then eluted from the silica with 10% methanol in ethyl acetate
10. 10
    OtroThe solvents were removed by rotary evaporation

Procedimiento

(4-Fluorophenyl) divinyl phosphine oxide (1.50 g, 7.65 mmol) and benzylamine (1.05 mL, 9.57 mmol) were dissolved in a mixture of 100 mL of THF and 100 mL of deionized water. The reaction mixture was heated at 90° C. overnight. The reaction mixture was concentrated by rotary evaporation and the product was extracted into dichloromethane and washed with saturated brine. The organic phase was dried with sodium sulfate, filtered, and concentrated by rotary evaporation to yield 2.52 g of crude product. Impurities were removed by passing a solution of the crude product in ethyl acetate through a plug of silica. The product was then eluted from the silica with 10% methanol in ethyl acetate. The solvents were removed by rotary evaporation to yield 1.89 g (6.24 mmol, 82%) of 1-benzyl-4-(4-fluorophenyl)-[1,4]azaphosphinane 4-oxide as a colorless oil. ESMS (m/z): (M+1)+ found, 304.

Fuente