تفاعل #50178
ord-22633109d3af45cc92382ba23aff32c0
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىThe volatiles were removed in vacuo
- 2workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
- 3workup.ADDITIONtreated with saturated aqueous NH4Cl
- 4تجفيفThe organic layer was dried over MgSO4
- 5ترشيحfiltered
- 6تركيزconcentrated in vacuo
- 7أخرىPurification 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.