반응 #1552032

ord-ee3221f44db8406fb02abcdbc40c0ddb

반응 방정식

CC(C)(C)[O-].[K+]
Potassium t-butoxide
[Cl-]
chloride
CCCC1CCC(C2CCC(=O)CC2)O1
4-(5-propyltetrahydro-2-furanyl)cyclohexanone
CCCC1CCC(C2CCC(C=O)CC2)O1
4-(5-propyltetrahydro-2-furanyl)cyclohexanecarboaldehyde
수율 76.2%

용매

반응 조건

온도
-20°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITthe stirring was continued for another 1 hour
  2. 2
    온도The reaction mixture was warmed to room temperature
  3. 3
    기타the mixture was separated
  4. 4
    workup.ADDITIONafter the addition of water (200 ml)
  5. 5
    건조The organic layer was dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  7. 7
    기타The residue was purified by silica gel chromatography (toluene:ethyl acetate=18:1)
  8. 8
    workup.DISSOLUTIONthe resultant product was dissolved in acetone (200 ml)
  9. 9
    workup.ADDITIONhydrochrolic acid (6 M) (200 ml) was added
  10. 10
    workup.WAITthe stirring was continued at room temperature for another 1 hour
  11. 11
    추출The mixture was extracted with toluene (100 ml)
  12. 12
    workup.ADDITIONafter the addition of water (200 ml)
  13. 13
    건조The solution was dried over anhydrous magnesium sulfate
  14. 14
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure

실험 절차

Methoxymethyltriphenylphophnium chloride (55.23 g) and THF (300 ml) were placed in a reaction vessel, and the solution was cooled to −20° C. Potassium t-butoxide (16.0 g) was added, and the stirring was continued for another 1 hour. Then, 4-(5-propyltetrahydro-2-furanyl)cyclohexanone (15 g) in a THF (100 ml) solution was added dropwise, and the stirring was continued for another 1 hour. The reaction mixture was warmed to room temperature, and the mixture was separated after the addition of water (200 ml). The organic layer was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (toluene:ethyl acetate=18:1), and the resultant product was dissolved in acetone (200 ml) and hydrochrolic acid (6 M) (200 ml) was added, and then the stirring was continued at room temperature for another 1 hour. The mixture was extracted with toluene (100 ml) after the addition of water (200 ml). The solution was dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure to give 4-(5-propyltetrahydro-2-furanyl)cyclohexanecarboaldehyde (12.2 g).

출처

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