反応式
[F:1][C:2]1[CH:3]=[C:4]([O:9]C)[CH:5]=[CH:6][C:7]=1[CH3:8].B(Br)(Br)Br>C(Cl)Cl>[F:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[CH:6][C:7]=1[CH3:8]参加物
4
反応条件
- 温度
- -70 °C
実験手順
To a −70° C. solution of 3-fluoro-4-methyl anisole (1.62 g; 11.6 mmol) in CH2Cl2 (10 mL) was added dropwise BBr3 (10 mL; 12 mmol). The reaction mixture was stirred at −70° C. for 10 min, then allowed to warm to 0° C. and stirred at 0° C. for 2 h. The reaction was allowed to warm to RT and concentrated in vacuo and the residue was partitioned between H2O and EtOAc. The organic phase was washed with H2O, dried (Na2SO4) and concentrated in vacuo to give 3-fluoro-4-methyl phenol (1.1 g; 75%) as an oil.
後処理
- temperatureto warm to 0° C.
- stirringstirred at 0° C. for 2 h
- temperatureto warm to RT
- concentrationconcentrated in vacuo
- customthe residue was partitioned between H2O and EtOAc
- washThe organic phase was washed with H2O
- dry with materialdried (Na2SO4)
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-8062bb8683d341519c4209c61902d06e
- 出典データセット
- uspto-grants-2005_07
- 特許番号
- US06919358B2
関連ノート
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