Acetic Acid → HCID 86726476、化合物
反応式
[Cl:1][C:2]1[N:6]([CH2:7][CH2:8][O:9][CH3:10])[N:5]=[CH:4][C:3]=1[N+:11]([O-])=O.C(O)(=O)C>O.[Fe]>[Cl:1][C:2]1[N:6]([CH2:7][CH2:8][O:9][CH3:10])[N:5]=[CH:4][C:3]=1[NH2:11]参加物
5
反応条件
- 温度
- 90 °C
実験手順
To a suspension of 5-chloro-1-(2-methoxyethyl)-4-nitro-1H-pyrazole (1 equiv) and iron dust (3 equiv) in water (0.51 M) was added acetic acid (2.6 equiv). The mixture was heated to 90° C. for 1.5 h, then cooled to room temperature. The reaction was quenched by addition of solid sodium bicarbonate and treated with ethyl acetate with continuous stirring. The mixture was filtered and the solid was rinsed with ethyl acetate. The combined filtrate was dried over sodium sulfate and concentrated. The crude product was purified by silica gel chromatography (1.5% MeOH in DCM) to provide the desired product (69% yield) as a brown oil. MS (ESI) m/z 176 [M+H]+.
後処理
- temperaturecooled to room temperature
- customThe reaction was quenched by addition of solid sodium bicarbonate
- additiontreated with ethyl acetate with continuous stirring
- filtrationThe mixture was filtered
- washthe solid was rinsed with ethyl acetate
- dry with materialThe combined filtrate was dried over sodium sulfate
- concentrationconcentrated
- customThe crude product was purified by silica gel chromatography (1.5% MeOH in DCM)
出典と根拠
- ORDレコード
- ord-7e9c9d2aa48b458cb48150781d735449
- 出典データセット
- uspto-grants-2016_08
- 特許番号
- US09428509B2
反応ノート
読み込み中…