Réaction #1552027

Équation de réaction

1-methoxymethylene-4-(3-propylcyclopentyl)cyclohexane

→

4-(3-propylcyclopentyl)cyclohexanecarboaldehyde

Rendement 93.8%

Solvants

Water

Conditions de réaction

Traitement

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

Mode opératoire

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).

Source