Reacción #1483060
ord-74255594308a4a4781df56b873f8e249
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1OtroSynthesized
- 2Temperaturawas heated
- 3Temperaturaat reflux
- 4Temperaturaat reflux
- 5Temperaturaheating
- 6Temperaturaat reflux
- 7workup.WAITAfter 4 hours
- 8Temperaturathe mixture was cooled to room temperature
- 9Extracciónextracted with ether (1×100 mL, 3×75 mL)
- 10OtroThe combined ether extracts were evaporated
- 11Otroplaced in a 120° C.
- 12Otro(ca. 15 minutes)
- 13TemperaturaThe mixture was cooled to room temperature
- 14workup.ADDITIONneutralized by addition of saturated NaHCO3 solution (150 mL)
- 15Extracciónthe resulting mixture extracted with CH2Cl2 (4×75 mL)
- 16SecadoThe combined CH2Cl2 solution was dried (MgSO4)
- 17Filtraciónfiltered
- 18Otroevaporated
Procedimiento
Synthesized according to Agosta and Smith, J. Org. Chem. 35: 3856 (1970) A mixture of 2-methyl-1,3-cyclopentanedione (10.025 g, 89.4 mmol, Aldrich), methyl iodide (6.0 mL, 96.4 mmol, Aldrich), and KOH (5.097 g, 90.8 mmol) in water (25 mL)/dioxane (75 mL) was heated at reflux. After 5 hours, a solution of KOH (2 g) and MeI (2.4 mL) in water (5 mL)/dioxane (15 mL) was added and after another 3 hours at reflux, the solution was stirred at room temperature overnight. A solution of KOH (2 g) and MeI (2.4 mL) in water (5 mL)/dioxane (15 mL) was added to the overnight reaction and heating at reflux. After 4 hours, the mixture was cooled to room temperature and extracted with ether (1×100 mL, 3×75 mL). The combined ether extracts were evaporated, the residue combined with 10% HCl (50 mL), and the resulting mixture placed in a 120° C. oil bath until it began boiling (ca. 15 minutes). The mixture was cooled to room temperature, neutralized by addition of saturated NaHCO3 solution (150 mL) and the resulting mixture extracted with CH2Cl2 (4×75 mL). The combined CH2Cl2 solution was dried (MgSO4), filtered and evaporated to leave a brown oil (10.474 g, 83 mmol, 93%) which was used directly in the next step.