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

HRID 1019742

반응식

HRID 1019742 반응식
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]

참가 물질

6

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온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-0da0360003694be6aaa3a15d4134a744
출처 데이터셋
uspto-grants-2014_05
특허 번호
US08716287B2

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