Réaction #8529

ord-c97f457d75724fd29a32be088e5f8a4c

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationAfter filtering off Pd—C and magnesium sulfate
  2. 2
    Concentrationthe obtained filtrate was concentrated under reduced pressure

Mode opératoire

2,3, 4-Trifluoroaniline (2.94 g) and ethyl pyruvate (2.32 g) were dissolved in methanol (30 ml). After adding 5% Pd—C (2.0 g) and anhydrous magnesium sulfate (2.65 g), the mixture was stirred at 50° C. in a hydrogen atmosphere for 16 hours. After filtering off Pd—C and magnesium sulfate, the obtained filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography (ethyl acetate-normal hexane=1:4) to thereby give the title compound (4.69 g) as a pale yellow oily substance. Various spectral data of this product was identical with those obtained in Example 7.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07087778B2uspto-grants-2006_08