反応式
[CH2:1]([CH:3]([C:9](=[O:11])[CH3:10])[C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH3:2].C(OCC)(=O)CC(C)=O>>[CH2:1]([CH:3]([CH:9]([OH:11])[CH3:10])[C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH3:2]参加物
3
実験手順
Ethyl 2-ethyl-3-hydroxybutyrate was prepared following the procedure as described in step 1) of Preparation Example 2, except for that ethyl 2-ethyl-3-oxo-butyrate was used to replace for ethyl acetoacetate. Yield 60%.
後処理
- customof Preparation Example 2
出典と根拠
- ORDレコード
- ord-9c943762f252480d883428cdefae8d39
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07351778B2
関連ノート
読み込み中…