Reaktion #1951069

ord-917456b9bf384d3691e9f398c783a47e

Reaktionsgleichung

O=P(Cl)(Cl)c1ccc(F)cc1
4-Fluorophenyl-phosphonic dichloride
C1CCOC1
THF
C=[CH][Mg][Br]
vinyl magnesium bromide
C1CCOC1
THF
[Cl-].[NH4+]
ammonium chloride
C=CP(=O)(C=C)c1ccc(F)cc1
4-fluoro-phenyl-divinyl-phosphine oxide
Ausbeute 83.0%

Reaktionsbedingungen

Temperatur
-70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

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, 1 M). The resulting solution was stirred for 90 minutes at −70° C. An aqueous solution of ammonium chloride (500 mL, 2 M) 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07625880B2uspto-grants-2009_12