反応式
[F:1][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[OH:11])[C:5]([OH:7])=[O:6].S(=O)(=O)(O)O.[CH2:17](O)[CH3:18]>>[CH2:17]([O:6][C:5](=[O:7])[C:4]1[CH:8]=[CH:9][C:10]([OH:11])=[C:2]([F:1])[CH:3]=1)[CH3:18]参加物
4
実験手順
A solution of 3-fluoro-4-hydroxy-benzoic acid (5.16 g, 33.1 mmol) in ethanol (100 ml) was treated with conc. sulphuric acid (5 ml), and the mixture heated at reflux for 4 days. The volatiles were removed in vacuo, and the aqueous residue was basified with saturated NaHCO3 and extracted twice with diethyl ether. The combined organic extracts were dried and concentrated in vacuo to yield the title compound (5.16 g, 85%).
後処理
- temperaturethe mixture heated
- temperatureat reflux for 4 days
- customThe volatiles were removed in vacuo
- extractionextracted twice with diethyl ether
- customThe combined organic extracts were dried
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-9c84b9f0d9cf4aa3ae0ff39ecb8f6250
- 出典データセット
- uspto-grants-2012_06
- 特許番号
- US08202858B2
関連ノート
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