Thionyl Chloride → 6,7-Dihydroxy-4-oxo-4H-1-benzopyran-3-carbonyl chloride
반응식
[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]참가 물질
3
실험 절차
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).
후처리
- 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
출처 및 근거
- ORD 기록
- ord-d7e05b2f497b4a1e9e3a50ae7b7835a9
- 출처 데이터셋
- uspto-grants-1983_11
- 특허 번호
- US04415567
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