cis-1-(tert-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinone → trans-3-Acetyl-1-(tert-butyldimethylsilyl)-4-trimethylsilylethynyl-2-azetidinone
反応式
[Si:1]([N:8]1[C@H:11]([C:12]#[C:13][Si:14]([CH3:17])([CH3:16])[CH3:15])[C@H:10]([C@H:18]([OH:20])[CH3:19])[C:9]1=[O:21])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]>C(OCC)(=O)C.[O-2].[O-2].[Mn+4]>[C:18]([C@H:10]1[C@H:11]([C:12]#[C:13][Si:14]([CH3:16])([CH3:15])[CH3:17])[N:8]([Si:1]([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2])[C:9]1=[O:21])(=[O:20])[CH3:19]参加物
4
反応条件
- 温度
- 25 °C
実験手順
Cis-1-(tert-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinone (0.15 g) is dissolved in ethyl acetate (20 ml), and 5 g of activated manganese dioxide is added, followed by stirring at 25° C. for 5 hours. The manganese dioxide is filtered off and the filtrate is concentrated to give trans-3-acetyl-1-(tert-butyldimethylsilyl)-4-trimethylsilylethynyl-2-azetidinone (0.14 g).
後処理
- filtrationThe manganese dioxide is filtered off
- concentrationthe filtrate is concentrated
出典と根拠
- ORDレコード
- ord-a70f07d30bb5450b8f1aafc39e97d89a
- 出典データセット
- uspto-grants-1989_07
- 特許番号
- US04845210
反応ノート
読み込み中…