Reacción #2348099

ord-a2fe6f079f0e4b3e90dd9d0d594c6450

Ecuación de reacción

[H][H]
hydrogen
CCCc1ccc(-c2ccc(C=CC3(F)C(F)=C(OCC)C=CC3C)cc2)cc1
compound ( 20 )
CCCc1ccc(-c2ccc(C=CC3(F)C(F)=C(OCC)C=CC3C)cc2)cc1
2-(2-(4-(4-propylphenyl)phenyl)ethenyl)-2,3-difluoro-4-ethoxytoluene
CCCc1ccc(-c2ccc(CCC3(F)C(F)=C(OCC)C=CC3C)cc2)cc1
2-(2-(4-(4-propylphenyl)phenyl) ethyl)-2,3-difluoro-4-ethoxytoluene
Rendimiento 81.9%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrowas not absorbed
  2. 2
    OtroPd/C was removed by filtration
  3. 3
    workup.DISTILLATIONthe solvent was distilled off
  4. 4
    OtroThe residue was purified by silica gel column chromatography and recrystallization

Procedimiento

0.36 g of Pd/C was added to 7.29 g of the compound (20) having been dissolved in 100 mL of toluene and 100 mL of Solmix, and under a hydrogen atmosphere, the mixture was stirred at room temperature until hydrogen was not absorbed. Pd/C was removed by filtration, and the solvent was distilled off. The residue was purified by silica gel column chromatography and recrystallization to obtain 6.00 g of 2-(2-(4-(4-propylphenyl)phenyl) ethyl)-2,3-difluoro-4-ethoxytoluene (Compound 1-3-3-22) as colorless crystals.

Fuente

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