Methyl iodide → 1,3-Cyclopentanedione, 2,2-dimethyl-

HRID 400320

반응식

HRID 400320 반응식
[CH3:1][CH:2]1[C:6](=[O:7])[CH2:5][CH2:4][C:3]1=[O:8].CI.[OH-].[K+].O1CCOC[CH2:14]1>O>[CH3:1][C:2]1([CH3:14])[C:6](=[O:7])[CH2:5][CH2:4][C:3]1=[O:8]

참가 물질

6

실험 절차

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.

후처리

  1. customSynthesized
  2. temperaturewas heated
  3. temperatureat reflux
  4. temperatureat reflux
  5. temperatureheating
  6. temperatureat reflux
  7. waitAfter 4 hours
  8. temperaturethe mixture was cooled to room temperature
  9. extractionextracted with ether (1×100 mL, 3×75 mL)
  10. customThe combined ether extracts were evaporated
  11. customplaced in a 120° C.
  12. custom(ca. 15 minutes)
  13. temperatureThe mixture was cooled to room temperature
  14. additionneutralized by addition of saturated NaHCO3 solution (150 mL)
  15. extractionthe resulting mixture extracted with CH2Cl2 (4×75 mL)
  16. dry with materialThe combined CH2Cl2 solution was dried (MgSO4)
  17. filtrationfiltered
  18. customevaporated

출처 및 근거

ORD 기록
ord-ba3c6c58135c408d9a7c738f4e528254
출처 데이터셋
uspto-grants-2014_06
특허 번호
US08741281B2

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