Sulfuric Acid → 3-Bromo-4-(trifluoromethoxy)aniline

HRID 1420827

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HRID 1420827 반응식
[F:1][C:2]([F:14])([F:13])[O:3][C:4]1[CH:9]=[CH:8][C:7]([N+:10]([O-])=O)=[CH:6][CH:5]=1.S(=O)(=O)(O)O.[Br:20]([O-])(=O)=O.[K+]>O>[Br:20][C:5]1[CH:6]=[C:7]([CH:8]=[CH:9][C:4]=1[O:3][C:2]([F:14])([F:13])[F:1])[NH2:10]

참가 물질

5

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온도
80 °C

실험 절차

4-Trifluoromethoxynitrobenzene (4.1 g) was suspended in water (16 ml) and concentrated sulfuric acid (16 ml) and warmed to 80° C. with stirring. Potassium bromate (3.7 g) was added portionwise over 3 h., and the mixture was heated at 80° C. for a further 2 h. The mixture was cooled to room temperature and poured onto ice (100 g). The mixture was extracted with ethyl acetate and the combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue) was dissolved in acetic acid (2.5 ml) and water (10 ml) and iron powder (2.0 g) was added. The mixture was heated under reflux for 2 h., cooled to room temperature and filtered through Celite™. The filtrate was extracted with ethyl acetate and the combined organic fractions were dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with hexane/EtOAc (3:1) to give the title compound as a yellow oil. 1H NMR (CDCl3) δ6.57 (1H, dd), 6.9 (1H, d), 7.06 (1H, dd).

후처리

  1. temperatureThe mixture was cooled to room temperature
  2. additionpoured onto ice (100 g)
  3. extractionThe mixture was extracted with ethyl acetate
  4. dry with materialthe combined organic fractions were dried (MgSO4)
  5. customthe solvent was evaporated under reduced pressure
  6. dissolutionThe residue) was dissolved in acetic acid (2.5 ml)
  7. additionwater (10 ml) and iron powder (2.0 g) was added
  8. temperatureThe mixture was heated
  9. temperatureunder reflux for 2 h.
  10. temperaturecooled to room temperature
  11. filtrationfiltered through Celite™
  12. extractionThe filtrate was extracted with ethyl acetate
  13. dry with materialthe combined organic fractions were dried (MgSO4)
  14. customthe solvent was evaporated under reduced pressure
  15. customThe residue was purified by column chromatography on silica gel
  16. washeluting with hexane/EtOAc (3:1)

출처 및 근거

ORD 기록
ord-98298d36b6314c6bb4c94699381b5099
출처 데이터셋
uspto-grants-2000_06
특허 번호
US06071927

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