反応式
C[O:2][C:3](=[O:10])[CH:4]=[C:5]([CH2:8][CH3:9])[CH2:6][CH3:7]>O1CCOCC1.[Pd]>[CH2:6]([CH:5]([CH2:8][CH3:9])[CH2:4][C:3]([OH:10])=[O:2])[CH3:7]参加物
4
実験手順
3-ethyl-pent-2-enoic acid methyl ester (150 mg, 1.056 mmol) was dissolved in dioxane (1 ml), and palladium 10% on activated carbon (30 mg) was added; the slurry was hydrogenated under pressure (40 p.s.i.) for 4 h. The carbon was filtered off and the filter was washed with dioxane (1 ml); 1N NaOH (2 ml) was added to the mixture which was left overnight at room temperature; after addition of 1N hydrochloric acid (3 ml), the product was extracted with ethyl acetate. The organic solution was dried over sodium sulfate, filtered and the solvent was removed under reduced pressure, obtaining 90 mg of 3-ethyl pentanoic acid as colourless oil. Yield 65.5%.
後処理
- filtrationThe carbon was filtered off
- washthe filter was washed with dioxane (1 ml)
- addition1N NaOH (2 ml) was added to the mixture which
- waitwas left overnight at room temperature
- additionafter addition of 1N hydrochloric acid (3 ml)
- extractionthe product was extracted with ethyl acetate
- dry with materialThe organic solution was dried over sodium sulfate
- filtrationfiltered
- customthe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-b7e825cb21e542f0a75df8c01cb76d61
- 出典データセット
- uspto-grants-2007_01
- 特許番号
- US07169890B2
関連ノート
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