反応 #94827
ord-dcbf84c204bc48bd8afb3fc0c8d16176
反応方程式
溶媒
反応条件
詳細条件
See reaction.notes.procedure_details.
後処理
- 1温度cooled to 0°-5° under nitrogen
- 2workup.STIRRINGThe mixture is stirred 1 hr
- 3その他quenched with water (10 ml)
- 4抽出The mixture is extracted with ethyl acetate (2×15 ml)
- 5乾燥dried over sodium sulfate
- 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.