Réaction #649597

ord-d336d5d68b4c4907a03c4ece191ebd93

Conditions de réaction

Température
-70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.STIRRINGstirred rapidly while the cold reaction mixture
  2. 2
    workup.ADDITIONwas added
  3. 3
    ExtractionThe product was extracted into dichloromethane
  4. 4
    Lavagewashed with saturated aqueous sodium bicarbonate
  5. 5
    SéchageThe organic phase was dried with sodium sulfate
  6. 6
    Filtrationfiltered
  7. 7
    Concentrationconcentrated by rotary evaporation

Mode opératoire

4-Fluorophenyl-phosphonic dichloride (6.86 g, 32.2 mmol) was dissolved in dry THF (50 mL), placed under a nitrogen atmosphere, and chilled to −70° C. To this stirred solution was added dropwise a solution of vinyl magnesium bromide in THF (80.5 mL, 1M). The resulting solution was stirred for 90 minutes at −70° C. An aqueous solution of ammonium chloride (500 mL, 2M) was chilled to 0° C. and stirred rapidly while the cold reaction mixture was added. The product was extracted into dichloromethane and washed with saturated aqueous sodium bicarbonate followed by water. The organic phase was dried with sodium sulfate, filtered, and concentrated by rotary evaporation to yield 5.214 g of 4-fluoro-phenyl-divinyl-phosphine oxide (26.6 mmol, 83%) as a white solid. 1H NMR (400 MHz, CDCl3) 7.80-7.71 (m, 2H); 7.25-7.18 (m 2H); 6.56-6.22 (m, 6H); ESMS (m/z): (M+1)+ found, 197.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08067395B2uspto-grants-2011_11