反応式
[OH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[CH:4][CH:3]=1.C(OP(=[S:18])(O)OCC)C>O>[OH:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]([NH2:7])=[S:18])=[CH:4][CH:3]=1参加物
反応条件
- 温度
- 80 °C
実験手順
In a round bottomed flask, 4-hydroxybenzonitrile (5.00 g, 41.9 mmol), diethylthiophosphoric acid (7.02 g, 41.9 mmol), and water (8 ml) were heated with stirring to about 80° C. for about thirty minutes. An additional 10 ml of water was then added to the suspension, and the reaction was heated for about another one hour. The mixture was then allowed to stir for about sixteen hours at room temperature and was then extracted with water and 1:1 ether/ethyl acetate. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting solid was purified by column chromatography (silica gel; hexanes to ethyl acetate). The product was isolated as a yellow solid (5.54 g, 87% yield). 1H NMR (CD3OD): δ6.74 (d, 2H, J=9.1 Hz), 7.83 (d, 2H, J=8.7 Hz).
後処理
- temperaturethe reaction was heated for about another one hour
- stirringto stir for about sixteen hours at room temperature
- extractionwas then extracted with water and 1:1 ether/ethyl acetate
- dry with materialThe combined organic extracts were dried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe resulting solid was purified by column chromatography (silica gel; hexanes to ethyl acetate)
出典と根拠
- ORDレコード
- ord-c6d3a934633245e097bf84e5d3a3d633
- 出典データセット
- uspto-grants-2004_03
- 特許番号
- US06706743B2
関連ノート
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