Réaction #81727

ord-20dec9601cad4b28adb26edc2aa51fff

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas heated
  2. 2
    Températureat reflux overnight
  3. 3
    ConcentrationThe reaction mixture was then concentrated
  4. 4
    workup.ADDITIONThe residue was diluted with water
  5. 5
    Extractionextracted with ethyl acetate
  6. 6
    ExtractionThe organic extract
  7. 7
    Lavagewas washed with brine
  8. 8
    Autredried
  9. 9
    Concentrationconcentrated
  10. 10
    LavageThe resulting solid was washed with CH3CN
  11. 11
    Autreisolated by filtration
  12. 12
    Autreto give

Mode opératoire

A mixture of methyl-17β-cyclohexylcarbonyl-estra-1,3,5(10)-triene-3-carboxylate (0.14 g, 0.34 mmol), K2CO3 (0.2 g, 1.45 mmol), water (3.0 mL) and methanol (30 mL) was heated at reflux overnight. The reaction mixture was then concentrated. The residue was diluted with water, acidified with dilute HCl and extracted with ethyl acetate. The organic extract was washed with brine, dried, and concentrated. The resulting solid was washed with CH3CN and isolated by filtration from boiling ethyl acetate to give, 0. 11 g of the title compound. mp 280°-285° C. (softened at 260° C.).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05618806uspto-grants-1997_04