Reaktion #2348102

ord-927888abcec1406db59e2ce9d1ab463f

Reaktionsgleichung

[H][H]
hydrogen
CCCCCc1ccc(-c2c(C=Cc3ccc(CCC)cc3)cc(C)c(F)c2F)cc1
compound ( 24 )
CCCCCc1ccc(-c2c(C=Cc3ccc(CCC)cc3)cc(C)c(F)c2F)cc1
2-(4-propylphenyl)ethenyl-2,3-difluoro-4-(4-pentylphenyl)toluene
CCCCCc1ccc(-c2c(CCc3ccc(CCC)cc3)cc(C)c(F)c2F)cc1
2-(4-propylphenyl)ethyl-2,3-difluoro-4-(4-pentylphenyl)toluene
Ausbeute 60.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

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

Vorschrift

0.33 g of Pd/C was added to 6.50 g of the compound (24) 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 3.94 g of 2-(4-propylphenyl)ethyl-2,3-difluoro-4-(4-pentylphenyl)toluene (Compound 1-2-3-3) as colorless crystals.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07846513B2uspto-grants-2010_12