反応式
[CH3:1][O:2][C:3]1[CH:11]=[C:7]([C:8]([OH:10])=[O:9])[C:6]([OH:12])=[CH:5][CH:4]=1.S(Cl)(Cl)=O.[CH2:17](O)[CH3:18]>>[CH2:17]([O:12][C:6]1[C:7](=[CH:11][C:3]([O:2][CH3:1])=[CH:4][CH:5]=1)[C:8]([OH:10])=[O:9])[CH3:18]参加物
実験手順
5-Methoxysalicylic acid (2.00 g) was suspended in ethanol (28 ml), and thionyl chloride (2.11 g) was gradually added dropwise to the suspension. Thereafter, the mixture was heated under reflux for 2 hr. The solvent was removed therefrom by distillation under the reduced pressure. Water was added to the residue, and the mixture was neutralized with a 20% aqueous sodium hydroxide solution and was then extracted with chloroform. The chloroform layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give ethyl 5-methoxysalicylic acid (1.37 g, yield 58%).
後処理
- temperatureThereafter, the mixture was heated
- temperatureunder reflux for 2 hr
- customThe solvent was removed
- distillationby distillation under the reduced pressure
- additionWater was added to the residue
- extractionwas then extracted with chloroform
- washThe chloroform layer was then washed with water and saturated brine
- dry with materialwas dried over anhydrous sodium sulfate
- customThe solvent was removed
- distillationby distillation under the reduced pressure
- customthe residue was purified by column chromatography
出典と根拠
- ORDレコード
- ord-4bfdb284ec3d478d801c03eb3cf59f4e
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07560558B2
関連ノート
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