Ethanol → 5-ethoxy-2-methyl-2H-pyran-3(6H)-one
反応式
[CH3:1][CH:2]1[C:7](=[O:8])[CH2:6][C:5](=[O:9])[CH2:4][O:3]1.[CH2:10](O)[CH3:11]>S(=O)(=O)(O)O>[CH2:10]([O:9][C:5]1[CH2:4][O:3][CH:2]([CH3:1])[C:7](=[O:8])[CH:6]=1)[CH3:11]参加物
4
実験手順
The product from Example 84C (3.0 g, 23 mmol) was dissolved in ethanol (50 mL), treated with concentrated sulfuric acid (5 drops), heated to reflux for 3 hours and concentrated. The residue was purified by chromatography eluting with 10:1 and then 5:1 and then 2:1 hexane:ethyl acetate to provide the title compound as the faster moving isomer.
後処理
- temperatureheated
- temperatureto reflux for 3 hours
- concentrationconcentrated
- customThe residue was purified by chromatography
- washeluting with 10:1
出典と根拠
- ORDレコード
- ord-13a9e2ec99674901be2c87a3f05fe087
- 出典データセット
- uspto-grants-2003_11
- 特許番号
- US06642222B2
反応ノート
読み込み中…