반응 #1552027

ord-d19722ba41da4debbe6166911ace8486

반응 방정식

CCCC1CCC(C2CCC(=COC)CC2)C1
1-methoxymethylene-4-(3-propylcyclopentyl)cyclohexane
CCCC1CCC(C2CCC(C=O)CC2)C1
4-(3-propylcyclopentyl)cyclohexanecarboaldehyde
수율 93.8%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타obtained in the first step, which
  2. 2
    workup.DISSOLUTIONwas dissolved in (200 ml)
  3. 3
    추출was extracted with toluene
  4. 4
    세척The combined organic layer was washed with water
  5. 5
    건조dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  7. 7
    workup.ADDITIONEthanol (200 ml) and toluene (50 ml) was added to the residue
  8. 8
    workup.ADDITIONa NaOH aqueous solution (20%) (30 ml) was added under ice-
  9. 9
    온도cooling
  10. 10
    workup.STIRRINGthe mixture was stirred at room temperature for another 3 hours
  11. 11
    workup.ADDITIONA saturated aqueous solution of ammonium chloride was added
  12. 12
    추출the mixture was extracted with toluene
  13. 13
    세척The combined organic layer was washed with water
  14. 14
    건조dried over anhydrous magnesium sulfate
  15. 15
    workup.DISTILLATIONthe toluene was distilled off under reduced pressure
  16. 16
    기타The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/20 by volume)

실험 절차

Hydrochrolic acid (1 M) (30 ml) was added to 1-methoxymethylene-4-(3-propylcyclopentyl)cyclohexane (17.0 g) obtained in the first step, which was dissolved in (200 ml), and the mixture was stirred at room temperature for 2 hours. Water (100 ml) was added to the mixture, which was extracted with toluene. The combined organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Ethanol (200 ml) and toluene (50 ml) was added to the residue, and a NaOH aqueous solution (20%) (30 ml) was added under ice-cooling, and the mixture was stirred at room temperature for another 3 hours. A saturated aqueous solution of ammonium chloride was added to neutralize and the mixture was extracted with toluene. The combined organic layer was washed with water, dried over anhydrous magnesium sulfate, and the toluene was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/20 by volume) to give 4-(3-propylcyclopentyl)cyclohexanecarboaldehyde (15.0 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08999197B2uspto-grants-2015_04