반응 #7553

ord-418ee189789f42de93dac3320c3963b2

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONby adding
  2. 2
    온도After the reaction mixture was cooled
  3. 3
    기타the organic layer was separated
  4. 4
    세척The organic layer was washed with a saturated aqueous sodium chloride solution
  5. 5
    건조dried over anhydrous magnesium sulfate
  6. 6
    workup.DISTILLATIONdistilled under reduced pressure
  7. 7
    기타to remove the solvent
  8. 8
    기타The residue was purified by a column chromatography (eluent; chloroform:methanol=75:1)

실험 절차

In a mixture of 0.4 mL of toluene and 7 mL of a 50% (W/V) aqueous sodium hydroxide solution was suspended 0.54 g of 2-(1-benzothiophen-5-yl)-1-ethanol, followed by adding thereto 1.45 g of 1-(3-chloropropyl)-3-(trityloxy)azetidine oxalate and 0.03 g of tetra-n-butylammonium bromide, and the resulting mixture was refluxed for 7 hours. After the reaction mixture was cooled, water and toluene were added thereto and the organic layer was separated. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and then distilled under reduced pressure to remove the solvent. The residue was purified by a column chromatography (eluent; chloroform:methanol=75:1) to obtain 0.59 g of 1-{3-[2-(1-benzothiophen-5-yl)ethoxy]propyl}-3-(trityloxy)azetidine as a light-yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087594B2uspto-grants-2006_08