Réaction #487502
ord-ba3c6c58135c408d9a7c738f4e528254
Équation de réaction
Réactifs
Conditions de réaction
Traitement
- 1AutreSynthesized
- 2Températurewas heated
- 3Températureat reflux
- 4Températureat reflux
- 5Températureheating
- 6Températureat reflux
- 7workup.WAITAfter 4 hours
- 8Températurethe mixture was cooled to room temperature
- 9Extractionextracted with ether (1×100 mL, 3×75 mL)
- 10AutreThe combined ether extracts were evaporated
- 11Autreplaced in a 120° C.
- 12Autre(ca. 15 minutes)
- 13TempératureThe mixture was cooled to room temperature
- 14workup.ADDITIONneutralized by addition of saturated NaHCO3 solution (150 mL)
- 15Extractionthe resulting mixture extracted with CH2Cl2 (4×75 mL)
- 16SéchageThe combined CH2Cl2 solution was dried (MgSO4)
- 17Filtrationfiltered
- 18Autreevaporated
Mode opératoire
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.