Thionyl Chloride → 6,7-Dihydroxy-4-oxo-4H-1-benzopyran-3-carbonyl chloride
反応式
[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[O:8][CH:7]=[C:6]([C:13](O)=[O:14])[C:5]2=[O:16].S(Cl)([Cl:19])=O>>[OH:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][C:11]=1[OH:12])[O:8][CH:7]=[C:6]([C:13]([Cl:19])=[O:14])[C:5]2=[O:16]参加物
3
実験手順
A mixture of 6,7-dihydroxychromone-3-carboxylic acid (888 mg, 4 mmol) and thionyl chloride (25 ml) was refluxed for one hour and the thionyl chloride was evaporated. After the addition of benzene, the mixture was evaporated again to dryness and the residue was triturated with dichloromethane to give the desired compound (719 mg).
後処理
- temperaturewas refluxed for one hour
- customthe thionyl chloride was evaporated
- additionAfter the addition of benzene
- customthe mixture was evaporated again to dryness
- customthe residue was triturated with dichloromethane
出典と根拠
- ORDレコード
- ord-28324460acf34701b013aa657da992b0
- 出典データセット
- uspto-grants-1981_08
- 特許番号
- US04285940
反応ノート
読み込み中…