反応式
[C:1]([O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][C:14]=1[O:15][C:16](=[O:18])[CH3:17])[O:11][CH:10]=[C:9]([CH:19]=[O:20])[C:8]2=[O:21])(=[O:3])[CH3:2].CC(C)=[O:24].OS(O)(=O)=O.O=[Cr](=O)=O.[Cr](O)(O)(=O)=O>CC(C)=O.S(=O)(=O)(O)O.O>[C:1]([O:4][C:5]1[CH:6]=[C:7]2[C:12](=[CH:13][C:14]=1[O:15][C:16](=[O:18])[CH3:17])[O:11][CH:10]=[C:9]([C:19]([OH:24])=[O:20])[C:8]2=[O:21])(=[O:3])[CH3:2]参加物
7
実験手順
6,7-Diacetoxychromone-3-carboxaldehyde (17.8 g) was dissolved in acetone (1 liter). To this solution was added dropwise with stirring Jones reagent (32.8 ml) which had been previously prepared by dissolving chromic acid (133.6 g) in concentrated sulfuric acid (115 ml) diluted with water to a volume of 500 ml.
後処理
- customhad been previously prepared
出典と根拠
- ORDレコード
- ord-1797cad0a35a4ba999469932486ad23a
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04344944
関連ノート
読み込み中…