Reacción #2348087

ord-f4b7e765bc3d465eb36be7b62ce67372

Ecuación de reacción

[Cl-].[NH4+]
ammonium chloride
CI
methyl iodide
[Mg]
magnesium
Fc1ccc(Br)cc1F
3,4-difluorobromobenzene
Cc1cccc(F)c1F
2,3-difluorotoluene

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONthe dropwise addition
  2. 2
    Temperaturathe mixture was refluxed for 1 hour
  3. 3
    workup.ADDITIONadded
  4. 4
    Temperaturaunder cooling with an ice bath
  5. 5
    Otroto terminate
  6. 6
    Otrothe reaction
  7. 7
    ExtracciónThe aqueous layer was extracted with diethyl ether, which
  8. 8
    workup.ADDITIONwas added to the organic layer
  9. 9
    Lavadothe organic layer was washed with a saturated saline
  10. 10
    Secadodried over anhydrous magnesium sulfate
  11. 11
    workup.DISTILLATIONThe organic layer was distilled

Procedimiento

Under a nitrogen atmosphere, 82.5 g of 3,4-difluorobromobenzene (1) dissolved in 150 mL of tetrahydrofuran (THF) was added dropwise to 12.5 g of dried magnesium, and after completing the dropwise addition, the mixture was refluxed for 1 hour. The resulting solution was added dropwise to 15 mL of THF having 91.5 g of methyl iodide and 12.3 g of copper(I) iodide added thereto under cooling with an ice bath. After stirring over night, a saturated ammonium chloride aqueous solution was added thereto to terminate the reaction. The aqueous layer was extracted with diethyl ether, which was added to the organic layer, and the organic layer was washed with a saturated saline and then dried over anhydrous magnesium sulfate. The organic layer was distilled to obtain 37.6 g of 2,3-difluorotoluene (2)

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07846513B2uspto-grants-2010_12