反応式
[S:1]1[CH:5]=[CH:4][C:3]([C:6]([OH:8])=[O:7])=[CH:2]1.S(=O)(=O)(O)O.[CH3:14]O>>[S:1]1[CH:5]=[CH:4][C:3]([C:6]([O:8][CH3:14])=[O:7])=[CH:2]1参加物
4
実験手順
3-thiophenecarboxylic acid (2.0 g) was dissolved in MeOH (27 mL) and concentrated sulphuric acid (1.5 mL) was added. The reaction mixture was refluxed for 3 hours and 30 min., then concentrated under reduced pressure. A saturated NaHCO3 solution was added and the mixture was extracted with ethyl acetate. The organic phase was dried over Na2SO4 and concentrated in vacuo to give 1.98 g of the title compound as a colourless liquid which was used without further purification.
後処理
- temperatureThe reaction mixture was refluxed for 3 hours and 30 min.
- concentrationconcentrated under reduced pressure
- additionA saturated NaHCO3 solution was added
- extractionthe mixture was extracted with ethyl acetate
- dry with materialThe organic phase was dried over Na2SO4
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-8d3e5106c7154efaadb5a663b4df7f11
- 出典データセット
- uspto-grants-2011_05
- 特許番号
- US07947683B2
関連ノート
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