Methanol → 5-Chloro-2-cyclohexyl-valeric acid
反応式
[OH-].[Na+].[Cl:3][CH2:4][CH2:5][CH2:6][CH:7]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)[C:8]([O:10]C)=[O:9].CO.O>C1COCC1.C(OCC)C>[Cl:3][CH2:4][CH2:5][CH2:6][CH:7]([CH:12]1[CH2:17][CH2:16][CH2:15][CH2:14][CH2:13]1)[C:8]([OH:10])=[O:9]参加物
反応条件
- 温度
- 60 °C
実験手順
A 5 N sodium hydroxide solution (2.5 ml) was added to a solution of methyl 5-chloro-2-cyclohexyl-valerate (1.00 g) in THF (3 ml)-methanol (6 ml). The reaction solution was stirred at room temperature for six hours and at 60° C. for further two hours. After allowing the reaction solution to cool, water and diethyl ether were added to the reaction solution, and the aqueous layer was separated. 5 N hydrochloric acid (2.6 ml) and ethyl acetate were added to the aqueous layer, and the organic layer was separated. The ethyl acetate extraction layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (heptane-ethyl acetate system) to obtain 5-chloro-2-cyclohexyl-valeric acid (287 mg).
後処理
- temperatureto cool
- customthe aqueous layer was separated
- addition5 N hydrochloric acid (2.6 ml) and ethyl acetate were added to the aqueous layer
- customthe organic layer was separated
- extractionThe ethyl acetate extraction layer
- washwas washed with brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe resulting residue was purified by silica gel column chromatography (heptane-ethyl acetate system)
出典と根拠
- ORDレコード
- ord-c0a60c69c739448980f831f0f726b8ee
- 出典データセット
- uspto-grants-2011_05
- 特許番号
- US07935815B2
反応ノート
読み込み中…