Sulfuric Acid → 2-(6-Hydroxy-1-benzofuran-3-yl)acetic acid
반응식
Cl[CH2:2][C:3]1[C:12]2[C:7](=[CH:8][C:9]([OH:13])=[CH:10][CH:11]=2)[O:6][C:5](=[O:14])[CH:4]=1.[OH-].[Na+].S(=O)(=O)(O)[OH:18]>>[OH:13][C:9]1[CH:10]=[CH:11][C:12]2[C:3]([CH2:4][C:5]([OH:14])=[O:18])=[CH:2][O:6][C:7]=2[CH:8]=1참가 물질
4
실험 절차
A mixture of the obtained 4-(chloromethyl)-7-hydroxy-2H-chromen-2-one (21.0 g, 21.0 mmol) and 1 M aqueous sodium hydroxide solution (1 L) was stirred at reflux for 2 h. The reaction mixture was acidified with concentrated sulfuric acid and extracted with ethyl acetate. The extract was washed with brine, dried over anhydrous sodium sulphate and concentrated to give (6-Hydroxy-1-benzofuran-3-yl)acetic acid (18.0 g, 93.75%).
후처리
- temperatureat reflux for 2 h
- extractionextracted with ethyl acetate
- washThe extract was washed with brine
- dry with materialdried over anhydrous sodium sulphate
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-8afc4a7fd3204a3387200e8307303e80
- 출처 데이터셋
- uspto-grants-2016_03
- 특허 번호
- US09278915B2
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