Reaktion #1527274

ord-b7c7544f31544eefa2a4537d3c0f4232

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthe reaction mixture was concentrated by evaporation under reduced pressure
  2. 2
    ExtraktionThe residue was then extracted with ethyl acetate
  3. 3
    WaschenThe extract was washed with water
  4. 4
    Trocknendried over anhydrous sodium sulfate
  5. 5
    Sonstigeevaporated to dryness under reduced pressure

Vorschrift

19.3 ml (0.0193 moles) of a 1N aqueous solution of sodium hydroxide were added t9 a solution of 5.05 g (0.0175 moles) of ethyl 2,4,5-trifluoro-3-trifluoromethoxybenzoate [(XXVIII), X=X'=F, R16 =C2H5O] [prepared as described in step (b) above] in 100 ml of ethanol, and the mixture was allowed to stand at room temperature for 2 hours. At the end of this time, 19.3 ml of 1N aqueous hydrochloric acid were added, and then the reaction mixture was concentrated by evaporation under reduced pressure. The residue was then extracted with ethyl acetate. The extract was washed with water, dried over anhydrous sodium sulfate, and evaporated to dryness under reduced pressure, to give 3.98 g of 2,4,5-trifluoro-3-trifluoromethoxybenzoic acid as a colorless powder.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05496951uspto-grants-1996_03