Reacción #1483060

ord-74255594308a4a4781df56b873f8e249

Ecuación de reacción

CC1C(=O)CCC1=O
2-methyl-1,3-cyclopentanedione
CI
methyl iodide
[K+].[OH-]
KOH
C1COCCO1
dioxane
[K+].[OH-]
KOH
CI
MeI
C1COCCO1
dioxane
[K+].[OH-]
KOH
CI
MeI
C1COCCO1
dioxane
CC1(C)C(=O)CCC1=O
oil
Rendimiento 93.0%
CC1(C)C(=O)CCC1=O
2,2-Dimethyl-cyclopentane-1,3-dione
Rendimiento 93.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroSynthesized
  2. 2
    Temperaturawas heated
  3. 3
    Temperaturaat reflux
  4. 4
    Temperaturaat reflux
  5. 5
    Temperaturaheating
  6. 6
    Temperaturaat reflux
  7. 7
    workup.WAITAfter 4 hours
  8. 8
    Temperaturathe mixture was cooled to room temperature
  9. 9
    Extracciónextracted with ether (1×100 mL, 3×75 mL)
  10. 10
    OtroThe combined ether extracts were evaporated
  11. 11
    Otroplaced in a 120° C.
  12. 12
    Otro(ca. 15 minutes)
  13. 13
    TemperaturaThe mixture was cooled to room temperature
  14. 14
    workup.ADDITIONneutralized by addition of saturated NaHCO3 solution (150 mL)
  15. 15
    Extracciónthe resulting mixture extracted with CH2Cl2 (4×75 mL)
  16. 16
    SecadoThe combined CH2Cl2 solution was dried (MgSO4)
  17. 17
    Filtraciónfiltered
  18. 18
    Otroevaporated

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08900571B2uspto-grants-2014_12