Reacción #1960504

ord-a16c8f531d7241509eb7d13751ffc34a

Ecuación de reacción

CCOc1cc2c(F)c(F)ccc2cc1[Si](C)(C)C
(3-ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilane
[Cs+].[F-]
caesium fluoride
CCOc1ccc2ccc(F)c(F)c2c1
7-ethoxy-1,2-difluoronaphthalene

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling
  2. 2
    Extracciónextracted a number of times with MTBE
  3. 3
    LavadoThe combined organic phases are washed with water and sat. sodium chloride soln
  4. 4
    Otro, and the solution is dried
  5. 5
    Otroafter removal of the solvent
  6. 6
    Otrois purified by column chromatography (SiO2, toluene:ethyl acetate=9:1)

Procedimiento

44.0 g (about 81.6 mmol) of (3-ethoxy-5,6-difluoronaphthalen-2-yl)trimethylsilane are stirred at 100° C. for 20 h together with 26.3 g (0.17 mol) of caesium fluoride in 300 ml of DMF. After cooling, the mixture is diluted with water and extracted a number of times with MTBE. The combined organic phases are washed with water and sat. sodium chloride soln., and the solution is dried using sodium sulfate. The brown oil remaining after removal of the solvent is purified by column chromatography (SiO2, toluene:ethyl acetate=9:1), giving 7-ethoxy-1,2-difluoronaphthalene as a brown oil.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08303844B2uspto-grants-2012_11