Hydrochloric Acid → ethyl 2-(4-cyano-1H-1,2,3-triazol-1-yl)acetate
反応式
[CH2:1]([O:3][C:4](=[O:9])[CH2:5][N:6]=[N+:7]=[N-:8])[CH3:2].Cl[C:11](=[CH2:14])[C:12]#[N:13].Cl>O>[CH2:1]([O:3][C:4](=[O:9])[CH2:5][N:6]1[CH:14]=[C:11]([C:12]#[N:13])[N:8]=[N:7]1)[CH3:2]参加物
実験手順
4.1 g (31.9 mmol) azidoacetic acid ethyl ester and 2.8 g (31.9 mmol) 2-chloroacrylonitrile are stirred in 32 ml water at a bath temperature of 80° C. for 16 h. After cooling to RT, the solution is rendered acid with 1 N hydrochloric acid and extracted with ethyl acetate. The organic phase is dried over sodium sulfate, filtered and concentrated in vacuo. 50 ml ethanol and 10 drops of conc. sulfuric acid are added to the residue and the mixture is stirred under reflux for 16 h. For working up, the reaction mixture is concentrated in vacuo, ethyl acetate is added to the residue, the suspension is washed with half-concentrated sodium bicarbonate solution and the organic phase is dried over sodium sulfate. The solvent is removed completely on a rotary evaporator and the solid is dried in vacuo.
後処理
- extractionextracted with ethyl acetate
- dry with materialThe organic phase is dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- addition50 ml ethanol and 10 drops of conc. sulfuric acid are added to the residue
- temperatureunder reflux for 16 h
- concentrationthe reaction mixture is concentrated in vacuo, ethyl acetate
- additionis added to the residue
- washthe suspension is washed with half-concentrated sodium bicarbonate solution
- dry with materialthe organic phase is dried over sodium sulfate
- customThe solvent is removed completely on a rotary evaporator
- customthe solid is dried in vacuo
出典と根拠
- ORDレコード
- ord-fdc2d8fb4ab048d780ac59f07e39fcb9
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08987261B2
反応ノート
読み込み中…