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-Dihydroxychromone-3-carboxylic acid (888 mg) and 25 ml of thionyl chloride were refluxed for one hour. Then, the thionyl chloride was removed by distillation, and after benzene was added, further distillation was conducted. Dichloromethane was added into the residue for solidification, whereby the desired product (719 mg) was obtained.
후처리
- customThen, the thionyl chloride was removed by distillation
- additionafter benzene was added
- distillationfurther distillation
- additionDichloromethane was added into the residue for solidification, whereby the desired product (719 mg)
- customwas obtained
출처 및 근거
- ORD 기록
- ord-63fbe7f0b4634b799b24b98090e97e11
- 출처 데이터셋
- uspto-grants-1982_08
- 특허 번호
- US04344944
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