Reaktion #965832

ord-7c0acb6cd8da4a8bb7a7bb0782a8dcdb

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe mixture was then purged with hydrogen
  2. 2
    FiltrationIt was then filtered
  3. 3
    Einengenfiltrate concentrated
  4. 4
    Sonstigeto give a residue which
  5. 5
    Sonstigewas purified by flash column chromatograph

Vorschrift

Charged [4-fluoro-2-[(E)-2-(4-fluorophenyl)ethenyl]phenyl]methanol (568 mg, 2.31 mmol, EXAMPLE 119, part A), Pd/C (65 mg) and methanol (6 mL) to a flask, the mixture was then purged with hydrogen, stirred at room temperature overnight. It was then filtered, filtrate concentrated to give a residue which was purified by flash column chromatograph to give 214 mg of the title compound (37%). 1H NMR (400 MHz, CDCl3): δ 1.42 (1H, t, J=5.2 Hz), 2.83-2.98 (4H, m), 4.59 (2H, d, J=5.6 Hz), 6.88-6.98 (4H, m), 7.08-7.11 (2H, m), 7.29-7.33 (1H, m).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08987461B2uspto-grants-2015_03