Réaction #1483060

ord-74255594308a4a4781df56b873f8e249

Équation de réaction

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
Rendement 93.0%
CC1(C)C(=O)CCC1=O
2,2-Dimethyl-cyclopentane-1,3-dione
Rendement 93.0%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08900571B2uspto-grants-2014_12