Réaction #81727
ord-20dec9601cad4b28adb26edc2aa51fff
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températurewas heated
- 2Températureat reflux overnight
- 3ConcentrationThe reaction mixture was then concentrated
- 4workup.ADDITIONThe residue was diluted with water
- 5Extractionextracted with ethyl acetate
- 6ExtractionThe organic extract
- 7Lavagewas washed with brine
- 8Autredried
- 9Concentrationconcentrated
- 10LavageThe resulting solid was washed with CH3CN
- 11Autreisolated by filtration
- 12Autreto 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.).