反応式
[CH3:1][C:2]1[O:8][C:7]([CH3:9])=[CH:6][C:4](=[O:5])[CH:3]=1>CCO>[CH3:9][CH:7]1[CH2:6][C:4](=[O:5])[CH2:3][CH:2]([CH3:1])[O:8]1参加物
3
実験手順
A solution of 2,6-dimethyl-γ-pyrone (17 g, Aldrich) in EtOH 95% (300 mL) was hydrogenated for 3 days under 70 psi. After filtration over celite, the solvent was evaporated and replaced by CH2Cl2. The solution was then treated with celite (30 g) and PCC (48.5 g). The suspension was stirred for 3 hr. and the reaction was diluted with Et2O (300 mL) and then filtered over a pad of celite. The filtrate was evaporated to dryness and the residual solution was then chromatographed using hexane/Et2O (1:1) to give the title compound.
後処理
- filtrationAfter filtration over celite
- customthe solvent was evaporated
- additionThe solution was then treated with celite (30 g) and PCC (48.5 g)
- additionand the reaction was diluted with Et2O (300 mL)
- filtrationfiltered over a pad of celite
- customThe filtrate was evaporated to dryness
- customthe residual solution was then chromatographed
出典と根拠
- ORDレコード
- ord-5f26eb2c965e46b1b3e67610bca06f60
- 出典データセット
- uspto-grants-1995_06
- 特許番号
- US05424320
関連ノート
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