Ethyl 2-(bicyclo[3.3.1]nonan-9-yl)acetate → 2-(Bicyclo[3.3.1]nonan-9-yl)acetic acid
反応式
[CH:1]12[CH:9]([CH2:10][C:11]([O:13]CC)=[O:12])[CH:5]([CH2:6][CH2:7][CH2:8]1)[CH2:4][CH2:3][CH2:2]2>CO.[OH-].[Na+]>[CH:5]12[CH:9]([CH2:10][C:11]([OH:13])=[O:12])[CH:1]([CH2:2][CH2:3][CH2:4]1)[CH2:8][CH2:7][CH2:6]2参加物
4
実験手順
To a solution of Example 56B (8.5 g 40.4 mmol) in methanol (100 mL), aqueous NaOH (50%, 25 mL) was added. The reaction was stirred at room temperature for 24 hours. Methanol was evaporated and the mixture was extracted with ether and then acidified with 6N HCl to pH 2. The mixture was extracted with ether (2×50 mL), the organic layer was dried with magnesium sulfate, filtered, and concentrated to afford the title compound.
後処理
- customMethanol was evaporated
- extractionthe mixture was extracted with ether
- extractionThe mixture was extracted with ether (2×50 mL)
- dry with materialthe organic layer was dried with magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-72d914873ea8410ea1a4165b6d632424
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08962639B2
反応ノート
読み込み中…