Reaktion #48069

ord-14b57bd0666e45aab253ce6c60b843fa

Reaktionsgleichung

Nc1ccc(F)c(Br)c1
3-bromo-4-fluorophenylamine
OB(O)C1CC1
cyclopropyl boronic acid
O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium phosphate
C1CCC(P(C2CCCCC2)C2CCCCC2)CC1
tricyclohexyl phosphine
Nc1ccc(F)c(C2CC2)c1
3-cyclopropyl-4-fluorophenylamine
Ausbeute 64.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe mixture was then cooled to RT
  2. 2
    Extraktionextracted with ether
  3. 3
    Waschenwashed with brine
  4. 4
    Trocknendried (MgSO4)
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated in vacuo
  7. 7
    Sonstigeto give a residue which
  8. 8
    Sonstigewas purified by flash column chromatography

Vorschrift

To a solution of 3-bromo-4-fluorophenylamine (synthesized as described in J. Org. Chem. 1981, 46, 2280-2286) (415 mg, 2.18 mmol), cyclopropyl boronic acid (244 mg, 2.84 mmol), potassium phosphate (1.62 g, 7.64 mmol), and tricyclohexyl phosphine (61 mg, 0.22 mmol) in toluene (10 ml) and water (0.5 ml) was added palladium acetate (25 mg, 0.11 mmol) and the reaction mixture was heated to 100° C. overnight. The mixture was then cooled to RT and diluted with water and extracted with ether. The organic phases were combined, washed with brine, dried (MgSO4), filtered and concentrated in vacuo to give a residue which was purified by flash column chromatography to give 3-cyclopropyl-4-fluorophenylamine (210 mg, 64%). MS (ISP) 152.2 (M+H)+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07745477B2uspto-grants-2010_06