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
6,7-Dihydroxychromon-3-carboxylic acid (888 mg) together with thionyl chloride (25 ml) were refluxed for one hour. Any unreacted thionyl chloride was then removed from the reaction mixture by distillation. Benzene was added to the residue, and the mixture was subjected to distillation. The residue was triturated with dichloromethane to obtain the desired product (719 mg).
後処理
- customAny unreacted thionyl chloride was then removed from the reaction mixture by distillation
- additionBenzene was added to the residue
- distillationthe mixture was subjected to distillation
- customThe residue was triturated with dichloromethane
出典と根拠
- ORDレコード
- ord-64df3025169449458472a78897e73697
- 出典データセット
- uspto-grants-1982_08
- 特許番号
- US04344944
反応ノート
読み込み中…