반응 #50178
ord-22633109d3af45cc92382ba23aff32c0
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상세 조건
See reaction.notes.procedure_details.
후처리
- 1기타The volatiles were removed in vacuo
- 2workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
- 3workup.ADDITIONtreated with saturated aqueous NH4Cl
- 4건조The organic layer was dried over MgSO4
- 5여과filtered
- 6농축concentrated in vacuo
- 7기타Purification 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.