Reaktion #1951070

Reaktionsgleichung

(4-Fluorophenyl) divinyl phosphine oxide

benzylamine

→

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

Ausbeute 82.0%

Lösungsmittel

THF

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   EinengenThe reaction mixture was concentrated by rotary evaporation
2. 2
   Extraktionthe product was extracted into dichloromethane
3. 3
   Waschenwashed with saturated brine
4. 4
   TrocknenThe organic phase was dried with sodium sulfate
5. 5
   Filtrationfiltered
6. 6
   Einengenconcentrated by rotary evaporation
7. 7
   Sonstigeto yield 2.52 g of crude product
8. 8
   SonstigeImpurities were removed
9. 9
   WaschenThe product was then eluted from the silica with 10% methanol in ethyl acetate
10. 10
    SonstigeThe solvents were removed by rotary evaporation

Vorschrift

(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.

Quelle