反応 #1552027

ord-d19722ba41da4debbe6166911ace8486

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他obtained in the first step, which
  2. 2
    workup.DISSOLUTIONwas dissolved in (200 ml)
  3. 3
    抽出was extracted with toluene
  4. 4
    洗浄The combined organic layer was washed with water
  5. 5
    乾燥dried 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
    温度cooling
  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
    抽出the mixture was extracted with toluene
  13. 13
    洗浄The combined organic layer was washed with water
  14. 14
    乾燥dried over anhydrous magnesium sulfate
  15. 15
    workup.DISTILLATIONthe toluene was distilled off under reduced pressure
  16. 16
    その他The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane=1/20 by volume)

実験手順

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).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08999197B2uspto-grants-2015_04