反応式
[Br:1][C:2]1[C:3]([F:10])=[C:4]([OH:9])[C:5]([Cl:8])=[CH:6][CH:7]=1.[C:11](=O)([O-])[O-].[K+].[K+].CI>C(#N)C>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([Cl:8])=[C:4]([O:9][CH3:11])[C:3]=1[F:10]参加物
5
反応条件
- 温度
- 85 °C
実験手順
To a stirred solution of 3-bromo-6-chloro-2-fluorophenol (4.2 g, 18.63 mmol) in acetonitrile (35 mL) was added potassium carbonate (5.15 g, 37.3 mmol) followed by the addition of methyl iodide (2.330 mL, 37.3 mmol) dropwise at rt. The reaction mixture was heated to 85° C. for 3 h. The volatiles were evaporated; water (50 mL) was added and the solution extracted with ethyl acetate (2×80 mL). The combined organic layers were washed with brine (100 mL), dried over sodium sulphate, and concentrated under reduced pressure. The crude material was taken to the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 7.20 (m, 1H), 7.05 (m, 1H), 3.98 (s, 3H).
後処理
- customThe volatiles were evaporated
- additionwater (50 mL) was added
- extractionthe solution extracted with ethyl acetate (2×80 mL)
- washThe combined organic layers were washed with brine (100 mL)
- dry with materialdried over sodium sulphate
- concentrationconcentrated under reduced pressure
- customThe crude material was taken to the next step without further purification
出典と根拠
- ORDレコード
- ord-d19569144d3d4a89b2e8a0fdb291a997
- 出典データセット
- uspto-grants-2015_03
- 特許番号
- US08969564B2
関連ノート
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