تفاعل #50178

ord-22633109d3af45cc92382ba23aff32c0

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe 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
    تجفيفThe organic layer was dried over MgSO4
  5. 5
    ترشيحfiltered
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىPurification by chromatography on silica gel (100 g, 30% ethyl acetate: hexanes)

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05426111uspto-grants-1995_06