Reacción #1951054

ord-3856480987e64374ba433607c49ad141

Ecuación de reacción

O=P(Cl)(Cl)c1ccccc1
phenylphosphonic dichloride
C1CCOC1
THF
C=[CH][Mg][Br]
Vinylmagnesium bromide
[Cl-].[NH4+]
NH4Cl
C=CP(=O)(C=C)c1ccccc1
divinyl-phenyl-phosphine oxide
Rendimiento 75.0%

Condiciones de reacción

Temperatura
-78°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONThe addition
  2. 2
    workup.STIRRINGAfter an additional 1 hour of stirring at −78° C.
  3. 3
    Otrothe cold reaction mixture
  4. 4
    ExtracciónThe mixture was extracted twice with CH2Cl2
  5. 5
    Lavadothe combined organic phase was washed with 1 M NaOH, brine
  6. 6
    Secadodried over Mg2SO4
  7. 7
    FiltraciónFiltration and solvent evaporation

Procedimiento

A solution of phenylphosphonic dichloride (29 mL, 200 mmol) dissolved in anhydrous THF (600 mL) was cooled to −78° C. and mechanically stirred under an atmosphere of dry nitrogen. Vinylmagnesium bromide (1 M in THF, 500 mL) was slowly added so that the temperature of the reaction mixture never exceeded −70° C. The addition took 2 hours. After an additional 1 hour of stirring at −78° C., the cold reaction mixture was poured directly into cold, saturated NH4Cl (1 L). The mixture was extracted twice with CH2Cl2 and the combined organic phase was washed with 1 M NaOH, brine, and then dried over Mg2SO4. Filtration and solvent evaporation provided divinyl-phenyl-phosphine oxide (26.8 g, 75%) as a viscous yellow oil that solidified upon standing. 1H NMR (400 MHz, DMSO-d6); δ 7.8-7.4 (m, 5H), 6.7 (m, 2H), 6.4-6.1 (m, 4H). 31P NMR (DMSO-d6); δ 17.0 (s).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07625880B2uspto-grants-2009_12