Réaction #1951070

Équation de réaction

(4-Fluorophenyl) divinyl phosphine oxide

benzylamine

→

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

Rendement 82.0%

Solvants

THF

water

Conditions de réaction

Traitement

1. 1
   ConcentrationThe reaction mixture was concentrated by rotary evaporation
2. 2
   Extractionthe product was extracted into dichloromethane
3. 3
   Lavagewashed with saturated brine
4. 4
   SéchageThe organic phase was dried with sodium sulfate
5. 5
   Filtrationfiltered
6. 6
   Concentrationconcentrated by rotary evaporation
7. 7
   Autreto yield 2.52 g of crude product
8. 8
   AutreImpurities were removed
9. 9
   LavageThe product was then eluted from the silica with 10% methanol in ethyl acetate
10. 10
    AutreThe solvents were removed by rotary evaporation

Mode opératoire

(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.

Source