반응 #50178

ord-22633109d3af45cc92382ba23aff32c0

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The volatiles were removed in vacuo
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  3. 3
    workup.ADDITIONtreated with saturated aqueous NH4Cl
  4. 4
    건조The organic layer was dried over MgSO4
  5. 5
    여과filtered
  6. 6
    농축concentrated in vacuo
  7. 7
    기타Purification by chromatography on silica gel (100 g, 30% ethyl acetate: hexanes)

실험 절차

To a solution of 4-methoxy-4-[3-(tetrahydropyran-2-yloxy)-prop-1-ynyl]tetrahydropyran (3.8 g, 14.8 mmol), prepared as in step 2, in methanol (50 mL), was added a catalytic amount of pyridinium p-toluenesulfonate (PPTS). The resulting yellow solution was stirred under nitrogen for 17 hours at ambient temperature. The volatiles were removed in vacuo and the residue was dissolved in ethyl acetate and treated with saturated aqueous NH4Cl. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo. Purification by chromatography on silica gel (100 g, 30% ethyl acetate: hexanes) provided 4-methoxy-4-(3-hydroxyprop-1-ynyl)tetrahydropyran (1.2 g, 47 %) as a colorless oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05426111uspto-grants-1995_06