Water → 1-Fluoro-3-(4-fluorophenoxy)-5-nitrobenzene

HRID 523945

反応式

HRID 523945 の反応式
F[C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[C:4]([F:11])[CH:3]=1.[C:12](=[O:15])([O-])[O-].[Cs+].[Cs+].O>FC1C=CC(O)=CC=1.CC(N(C)C)=O.C(OCC)(=O)C>[F:11][C:4]1[CH:5]=[C:6]([N+:8]([O-:10])=[O:9])[CH:7]=[C:2]([O:15][C:12]2[CH:6]=[CH:5][C:4]([F:11])=[CH:3][CH:2]=2)[CH:3]=1

参加物

7

反応条件

温度
50 °C

実験手順

Under an argon atmosphere and at room temperature, in a 500-mL pear-shaped evaporating flask, 4-fluorophenol (18.5 g) and 1,3-difluoro-5-nitrobenzene (25.0 g) were dissolved in DMA (300 mL). The reaction system was added with cesium carbonate (15.3 g) and stirred. The reaction system was then heated to 50° C., stirred for 3 hours, then heated to 65° C., stirred for 1 hour and further heated to 85° C. and stirred for 1 hour. The reaction solution was allowed to cool to room temperature, diluted with ethyl acetate and added with water to extract an organic layer. The aqueous layer was added with ethyl acetate to extract an organic layer. The organic layer was combined and washed with water and a saturated sodium chloride solution and the solvent was then distilled off under reduced pressure to give the titled compound (35.0 g) having the following physical properties.

後処理

  1. stirringstirred for 3 hours
  2. temperatureheated to 65° C.
  3. stirringstirred for 1 hour
  4. temperaturefurther heated to 85° C.
  5. stirringstirred for 1 hour
  6. temperatureto cool to room temperature
  7. extractionto extract an organic layer
  8. additionThe aqueous layer was added with ethyl acetate
  9. extractionto extract an organic layer
  10. washwashed with water
  11. distillationa saturated sodium chloride solution and the solvent was then distilled off under reduced pressure

出典と根拠

ORDレコード
ord-6de27b14a04545598a42b522b5932720
出典データセット
uspto-grants-2016_05
特許番号
US09340499B2

関連ノート

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