Acetic Acid → 2,2-Dimethyl-4-oxocyclopentane-1-carboxylic acid
反応式
[CH3:1][C:2]1([CH3:8])[CH2:6][C:5](=[O:7])[CH:4]=[CH:3]1.[C-]#N.[K+].C[C:13]([OH:15])=[O:14]>CCO.O>[CH3:1][C:2]1([CH3:8])[CH2:6][C:5](=[O:7])[CH2:4][CH:3]1[C:13]([OH:15])=[O:14]参加物
反応条件
- 温度
- 40 °C
実験手順
To a solution of 4,4-dimethylcyclopent-2-enone (2.0 g, 18 mmol) in EtOH (50 mL), water (7.5 mL) and AcOH (1.5 mL) was added potassium cyanide (2.36 g, 36.3 mmol). The reaction mixture was heated to about 40° C. and after about 15 h the reaction mixture was concentrated under reduced pressure. The residue was diluted with EtOAc (50 mL) and washed with brine. The organic layer was separated, dried over anhydrous Na2SO4, filtered, and concentrated. The residue was dissolved in aqueous HCl (6N, 50 mL) and heated to reflux. After about 3 days the reaction mixture was cooled to room temperature and concentrated under reduced pressure to provide 2,2-dimethyl-4-oxocyclopentanecarboxylic acid (3.7 g, 90%, ˜70% purity by 1H NMR) that was carried on without additional purification: LC/MS (Table 2, Method a) Rt=1.30 min; MS m/z: 155 (M−H)−.
後処理
- concentrationwas concentrated under reduced pressure
- additionThe residue was diluted with EtOAc (50 mL)
- washwashed with brine
- customThe organic layer was separated
- dry with materialdried over anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated
- dissolutionThe residue was dissolved in aqueous HCl (6N, 50 mL)
- temperatureheated to reflux
- temperatureAfter about 3 days the reaction mixture was cooled to room temperature
- concentrationconcentrated under reduced pressure
出典と根拠
- ORDレコード
- ord-e122ff7ed0ec4f6a95744a1a8b88209b
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08962629B2
反応ノート
読み込み中…