Potassium Cyanide → 3-Chloro-2-iodobenzeneacetonitrile
反応式
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([Cl:9])[C:4]=1[I:10].[C-:11]#[N:12].[K+]>CCO.O>[Cl:9][C:5]1[C:4]([I:10])=[C:3]([CH2:2][C:11]#[N:12])[CH:8]=[CH:7][CH:6]=1参加物
5
実験手順
A mixture of 1-(bromomethyl)-3-chloro-2-iodobenzene (7 g, 21 mmol) in 100 mL EtOH was treated with a solution of potassium cyanide (2 mL, 42 mmol) in 20 mL water. The mixture was refluxed for 2.5 hours. The mixture was cooled to room temperature and concentrated. The residue was diluted with 200 mL EtOAc, washed with water (2×50 mL), saturated NaCl (50 mL), dried over anhydrous sodium sulfate and concentrated. The crude product was purified by column chromatography (20% EtOAc/hexane) to give 3.2 g pale yellow solid. MS m/e: (M+H)+ 278.
後処理
- temperatureThe mixture was refluxed for 2.5 hours
- concentrationconcentrated
- additionThe residue was diluted with 200 mL EtOAc
- washwashed with water (2×50 mL), saturated NaCl (50 mL)
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated
- customThe crude product was purified by column chromatography (20% EtOAc/hexane)
出典と根拠
- ORDレコード
- ord-d8e7260cdeb048db8aec7358a53e8f26
- 出典データセット
- uspto-grants-2009_12
- 特許番号
- US07635715B2
反応ノート
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