反应 #2446066

ord-09de49fe9d4c4bf09a0a517c03ab7cbb

反应方程式

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

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

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

实验过程

Hydrochloric 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).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08685274B2uspto-grants-2014_04