反応式
[CH3:1][C:2]1[O:3][C:4]([CH3:9])=[CH:5][C:6](=[O:8])[CH:7]=1.[H][H]>C(O)C>[CH3:1][CH:2]1[CH2:7][CH:6]([OH:8])[CH2:5][CH:4]([CH3:9])[O:3]1参加物
4
実験手順
2,6-Dimethyl-4H-pyran-4-one (5.0 g) in ethanol (40 ml) was hydrogenated under 10% Pd—C (0.5 g) at 10 bar of hydrogen for 2 days. The solution was then evaporated to an oil which was purified by silica-gel MPLC [using a 1:1 mixture of ethyl acetate and hexane as eluant] to give the title product (3.71 g, 74%).
後処理
- customThe solution was then evaporated to an oil which
- customwas purified by silica-gel MPLC [
- additiona 1:1 mixture of ethyl acetate and hexane as eluant]
出典と根拠
- ORDレコード
- ord-24bf56278c174f3181d06e5553761ff1
- 出典データセット
- uspto-grants-2002_04
- 特許番号
- US06365751B1
関連ノート
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