反応 #1258

ord-aa775880ee5b480896f2619381c4dc7e

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    ろ過The reaction mixture was cleared of silver oxide by filtration
  2. 2
    濃縮concentrated under reduced pressure
  3. 3
    その他the residue was purified by silica gel column chromatography

実験手順

1.0 g of (-)-2-(4-(3-hydroxy-4,4,4-trifluoro-1-butenyl) phenyl)-5-decyloxypyrimidine was dissolved in 5 ml of butyl iodide. The solution was added with 3 g of silver oxide and stirred at 25°-30° C. for 4 days. The reaction mixture was cleared of silver oxide by filtration and concentrated under reduced pressure, and the residue was purified by silica gel column chromatography using toluene/ethyl acetate as eluent to obtain 0.98 g of (-)-2-(4-(3-butoxy-4,4,4-trifluoro-1-butenyl)phenyl)-5-decyloxypyrimidine.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723610uspto-grants-1998_03