Réaction #64060

ord-5a6c27d9b39946cfb6545476b452430c

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Filtrationfiltered
  2. 2
    Lavagewashed with water
  3. 3
    Séchagedried over anhydrous sodium sulfate
  4. 4
    AutreEvaporation of the solvent

Mode opératoire

Palladium on activated carbon (0.30 g), followed by concentrated hydrochloric acid (20 ml), were added to a solution of 5-(4-benzyloxy-2,6-dimethylphenyl)-3-hydroxy-2-propionylcyclohex-2-en-1-one (see Example 36) (3.22 g; 8.5 mmole) in ethyl acetate (200 ml). The mixture was hydrogenated at atmospheric pressure for 3 hours, then filtered, washed with water and dried over anhydrous sodium sulfate. Evaporation of the solvent gave 5-(2,6-dimethyl-4-hydroxyphenyl)-3-hydroxy-2-propionylcyclohex-2-en-1-one (2.45 g; 100%) as a yellow oil.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04767879uspto-grants-1988_08