Methanol → 1-Chloro-2-fluoro-4-methoxy-5-nitrobenzene

HRID 1019742ノート

反応式

HRID 1019742 の反応式
C[C:2](C)([O-:4])C.[K+].CO.[Cl:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[C:13](F)=[CH:12][C:11]=1[F:20].O>CN(C=O)C>[Cl:9][C:10]1[CH:15]=[C:14]([N+:16]([O-:18])=[O:17])[C:13]([O:4][CH3:2])=[CH:12][C:11]=1[F:20]

参加物

6

反応条件

温度
0 °C

実験手順

To a mixture of potassium tert-butoxide (3.0 g, 26.9 mmol) in DMF (20 mL), methanol (0.79 g, 24.8 mmol) was added at 0° C. The reaction mixture was stirred at 0° C. for 15 minutes then a solution of 1-chloro-2,4-difluoro-5-nitrobenzene (4.0 g, 20.7 mmol) in DMF (20 mL) was added at 0° C. and the reaction mass stirred for 3 hours at room temperature. Water (200 mL) was added to the reaction mixture and reaction mass was extracted with EtOAc (3×50 mL). The combined organic extracts were washed with water (80 mL), brine (80 mL), dried (Na2SO4) and concentrated under reduced pressure. The product was purified by column chromatography on neutral silica gel using 20-25% EtOAc in hexane to give the desired product (3 g, 71%) as a solid.

後処理

  1. additionwas added at 0° C
  2. stirringthe reaction mass stirred for 3 hours at room temperature
  3. extractionwas extracted with EtOAc (3×50 mL)
  4. washThe combined organic extracts were washed with water (80 mL), brine (80 mL)
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated under reduced pressure
  7. customThe product was purified by column chromatography on neutral silica gel using 20-25% EtOAc in hexane

出典と根拠

ORDレコード
ord-0da0360003694be6aaa3a15d4134a744
出典データセット
uspto-grants-2014_05
特許番号
US08716287B2

反応ノート

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