반응 #2446070

ord-b57073c8b7ee4be3a59fdd28fec7cb49

반응 방정식

Cc1ccccc1
Toluene
Cc1ccc(S(=O)(=O)O)cc1.O
p-toluenesulfonic acid monohydrate
CCCC1CCC(C2CCC(O)(c3ccc(OCC)c(F)c3F)CC2)C1
1-(4-ethoxy-2,3-difluorophenyl)-4-(3-propylcyclopentyl)cyclohexanol
CCCC1CCC(C2CC=C(c3ccc(OCC)c(F)c3F)CC2)C1
1-ethoxy-2,3-difluoro-4-(4-(3-propylcyclopentyl)cyclohex-1-enyl)benzene
수율 82.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타obtained in the first step, in a reaction vessel
  2. 2
    기타equipped with a Dean-Stark apparatus under an atmosphere of nitrogen
  3. 3
    온도The mixture was refluxed for 1.5 hour
  4. 4
    기타was removed with a Dean-Stark apparatus
  5. 5
    세척the reaction solution was washed with water
  6. 6
    건조dried over anhydrous magnesium sulfate
  7. 7
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  8. 8
    기타The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane= 1/10 by volume)

실험 절차

Toluene (50 ml) and p-toluenesulfonic acid monohydrate (0.15 g) were added to 1-(4-ethoxy-2,3-difluorophenyl)-4-(3-propylcyclopentyl)cyclohexanol (5.0 g) obtained in the first step, in a reaction vessel equipped with a Dean-Stark apparatus under an atmosphere of nitrogen. The mixture was refluxed for 1.5 hour, while forming water was removed with a Dean-Stark apparatus. After the mixture had been cooled to room temperature, the reaction solution was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate/n-heptane= 1/10 by volume) to give 1-ethoxy-2,3-difluoro-4-(4-(3-propylcyclopentyl)cyclohex-1-enyl)benzene (3.9 g).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08685274B2uspto-grants-2014_04