Hydrochloric Acid → 4-Pentyl-3-cyclohexenylcarboxylic acid
反応式
[CH2:1]([C:6]1[CH2:11][CH2:10][CH:9]([C:12]([O:14]CC)=[O:13])[CH2:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5].[OH-].[K+].Cl>O>[CH2:1]([C:6]1[CH2:11][CH2:10][CH:9]([C:12]([OH:14])=[O:13])[CH2:8][CH:7]=1)[CH2:2][CH2:3][CH2:4][CH3:5]参加物
5
実験手順
Ethyl 4-pentyl-3-cyclohexen-l-carboxylate (3.0 g) is added to a solution of water (27 ml) and potassium hydroxide (2.6 g). The mixture is stirred under reflux for 16 hours. The reaction mixture is then neutralized with a mixture of concentrated HCl (40 ml), water (40 ml), and ice (ca. 40 g), and the mixture extracted with dichloromethane (100 ml). The combined organic extracts are dried with sodium sulfate, and the solution concentrated in vacuo. The solid is recrystallized from a mixture of methanol (70 ml) and water (25 ml), resulting in the product, 4-pentyl-3-cyclohexen-1-carboxylic acid.
後処理
- temperatureunder reflux for 16 hours
- extractionthe mixture extracted with dichloromethane (100 ml)
- dry with materialThe combined organic extracts are dried with sodium sulfate
- concentrationthe solution concentrated in vacuo
- customThe solid is recrystallized from a mixture of methanol (70 ml) and water (25 ml)
出典と根拠
- ORDレコード
- ord-9095b4c11c8645fc9a09445c02a9bf68
- 出典データセット
- uspto-grants-1993_12
- 特許番号
- US05271864
反応ノート
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