反応 #94827

ord-dcbf84c204bc48bd8afb3fc0c8d16176

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度cooled to 0°-5° under nitrogen
  2. 2
    workup.STIRRINGThe mixture is stirred 1 hr
  3. 3
    その他quenched with water (10 ml)
  4. 4
    抽出The mixture is extracted with ethyl acetate (2×15 ml)
  5. 5
    乾燥dried over sodium sulfate
  6. 6
    濃縮concentrated under reduced pressure

実験手順

21-Chloro-21-(phenylsulfinyl)pregna-4,9(11),17(20),20-tetraen-3-one, (V, Example 2, 100 mg) and THF (1 ml) are slurried and cooled to 0°-5° under nitrogen. Sodium methoxide in methanol (25%, 0.05 ml) is added with stirring. The mixture is stirred 1 hr and then quenched with water (10 ml). The mixture is extracted with ethyl acetate (2×15 ml). The organic extracts are combined, backwashed with water (10 ml), dried over sodium sulfate and concentrated under reduced pressure to give the title compound.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US04342702uspto-grants-1982_08