Potassium Hydroxide → HCID 90103465、化合物
反応式
[OH-].[K+].[CH2:3]([O:5][C:6](=[O:17])[CH2:7][CH:8]([CH2:13][N+]([O-])=O)[C:9]([F:12])([F:11])[F:10])[CH3:4].[O-:18]S([O-])(=O)=O.[Mg+2].[O-][Mn](=O)(=O)=O.[K+]>C1COCC1.O>[CH2:3]([O:5][C:6](=[O:17])[CH2:7][CH:8]([CH:13]=[O:18])[C:9]([F:12])([F:11])[F:10])[CH3:4]参加物
反応条件
- 温度
- 0 °C
実験手順
In a 100 mL round-bottomed flask, KOH (356 mg, 5.45 mmol) was combined with H2O (50 ml) to give a colorless solution and cooled to 0° C. 4,4,4-Trifluoro-3-nitromethyl-butyric acid ethyl ester (1.25 g, 5.45 mmol) in 10 ml THF was added and the resulting reaction mixture was stirred for 20 min. This was followed by addition of MgSO4 (657 mg, 5.45 mmol) in 5 ml of H2O then by KMnO4 (862 mg, 5.45 mmol) in 30 ml of H2O. The resulting reaction mixture was stirred for 30 min, filtered through celite and the celite cake washed with CH2Cl2. The combined filtrate and washes were washed with brine, dried over Na2SO4, filtered and concentrated to afford 4,4,4-trifluoro-3-formyl-butyric acid ethyl ester as a liquid which was used without purification.
後処理
- customto give a colorless solution
- customthe resulting reaction mixture
- customThe resulting reaction mixture
- stirringwas stirred for 30 min
- filtrationfiltered through celite
- washthe celite cake washed with CH2Cl2
- washThe combined filtrate and washes were washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-955962637e704064a17b9764098c1f08
- 出典データセット
- uspto-grants-2016_07
- 特許番号
- US09388172B2
反応ノート
読み込み中…