Реакция #1509613

ord-309a747c3cab4289943c11a59163df16

Уравнение реакции

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

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеSynthesized
  2. 2
    Температураwas heated
  3. 3
    Температураat reflux
  4. 4
    Температураat reflux
  5. 5
    Температураheating
  6. 6
    Температураat reflux
  7. 7
    workup.WAITAfter 4 hours
  8. 8
    Температураthe mixture was cooled to room temperature
  9. 9
    Экстракцияextracted with ether (1×100 mL, 3×75 mL)
  10. 10
    ДругоеThe combined ether extracts were evaporated
  11. 11
    Другоеplaced in a 120° C.
  12. 12
    Другое(ca. 15 minutes)
  13. 13
    ТемператураThe mixture was cooled to room temperature
  14. 14
    workup.ADDITIONneutralized by addition of saturated NaHCO3 solution (150 mL)
  15. 15
    Экстракцияthe resulting mixture extracted with CH2Cl2 (4×75 mL)
  16. 16
    СушкаThe combined CH2Cl2 solution was dried (MgSO4)
  17. 17
    Фильтрацияfiltered
  18. 18
    Другоеevaporated

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08926963B2uspto-grants-2015_01