Diethyl Oxalate → 6-fluoro-4-oxo-4H-chromene-2-carboxylic acid
反応式
[CH3:1][C:2]([C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[CH:6][C:5]=1[OH:11])=[O:3].CC(C)([O-])C.[K+].[C:18](OCC)(=O)[C:19]([O:21]CC)=[O:20]>>[F:10][C:8]1[CH:7]=[CH:6][C:5]2[O:11][C:18]([C:19]([OH:21])=[O:20])=[CH:1][C:2](=[O:3])[C:4]=2[CH:9]=1参加物
4
実験手順
5-Fluoro-2-hydroxyacetophenone (II) was treated with potassium tertiary butoxide and diethyl oxalate to give 6-fluoro-4-oxo-4H-1-benzopyran-2-carboxylic acid (III) according to Reaction 1 as given below by a known process (JP 2218675).
出典と根拠
- ORDレコード
- ord-d3ea7fc41cc242e8973767fca59050ba
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08633241B2
反応ノート
読み込み中…