تفاعل #952076
ord-70e59825b90449f393151efa1d74c91d
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1أخرىpartitioned between ether and water
- 2أخرىThe organic layers were dried
- 3أخرىevaporated
- 4أخرىto yield 0.5 g of a crude product
- 5أخرىThis was purified via chromatography on silica gel using 25% ethyl acetate in hexanes as the eluant
الإجراء التجريبي
To a solution of the product of step (b) (0.49 g, 1.26 mmol) in 5 ml THF at -20° C. under nitrogen was added a slurry of benzyl oxide (73.78 mmol) generated from benzyl alcohol and oil free sodium hydride in 2 ml THF. The reaction mixture was allowed to warm to room temperature and stirred for several hours, then partitioned between ether and water. The organic layers were dried and evaporated to yield 0.5 g of a crude product. This was purified via chromatography on silica gel using 25% ethyl acetate in hexanes as the eluant to give 0.177 g of 2,4-dibenzyloxy-3-(3-ethoxy-2-methyl-4-methylsulfonylbenzoyl)pyridine, a viscous yellow oil.