cis-1-(tert-butyldimethylsilyl)-3-[(R)-1-hydroxyethyl]-4-trimethylsilylethynyl-2-azetidinone → trans-3-Acetyl-1-(tert-butyldimethylsilyl)-4-trimethylsilylethynyl-2-azetidinone

HRID 231238ノート

反応式

HRID 231238 の反応式
[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

  1. filtrationThe manganese dioxide is filtered off
  2. 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…