تفاعل #2446066

ord-09de49fe9d4c4bf09a0a517c03ab7cbb

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08685274B2uspto-grants-2014_04