تفاعل #952076

ord-70e59825b90449f393151efa1d74c91d

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىpartitioned between ether and water
  2. 2
    أخرىThe organic layers were dried
  3. 3
    أخرىevaporated
  4. 4
    أخرىto yield 0.5 g of a crude product
  5. 5
    أخرىThis 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05565413uspto-grants-1996_10