Boron tribromide → 3-Fluoro-4-methylphenol

HRID 480655

反応式

HRID 480655 の反応式
[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

  1. temperatureto warm to 0° C.
  2. stirringstirred at 0° C. for 2 h
  3. temperatureto warm to RT
  4. concentrationconcentrated in vacuo
  5. customthe residue was partitioned between H2O and EtOAc
  6. washThe organic phase was washed with H2O
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-773cb28411f74f21b62a1ac81b99ead0
出典データセット
uspto-grants-2003_11
特許番号
US06653314B2

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