Carbon Dioxide → 4-methoxy-2-(trifluoromethyl)benzoic Acid

HRID 2081329

반응식

HRID 2081329 반응식
[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[C:5]([O:10][CH3:11])[CH:6]=[CH:7][C:8]=1Br.[Mg].II.[C:17](=[O:19])=[O:18].Cl>O1CCCC1>[F:1][C:2]([F:13])([F:12])[C:3]1[CH:4]=[C:5]([O:10][CH3:11])[CH:6]=[CH:7][C:8]=1[C:17]([OH:19])=[O:18]

참가 물질

7

실험 절차

Dry tetrahydrofuran (10 ml) was added to 3-trifluoromethyl-4-bromo-1-methoxybenzene (compound III) (4.4 g) and metallic magnesium (0.41 g) and thereto was further added a catalytic amount of iodine, followed by refluxing for 1.5 hours with stirring. After the temperature was returned to room temperature, to the mixture was slowly added dropwise a solution prepared by adding dry ice (30 g) to dry tetrahydrofuran (10 ml) at -40° C. or lower. The temperature was returned to room temperature and then the reaction was allowed to proceed for further 2 hours. Then, the reaction mixture was added to 1N hydrochloric acid (50 ml) to stop the reaction and repeatedly extracted with ethyl acetate. The ethyl acetate layer was sufficiently washed with water and dried by adding anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure and then, the resulting solid was recrystallized from methylene chloride to obtain 2-trifluoromethyl-4-methoxybenzoic acid (compound IV, 1.5 g).

후처리

  1. temperatureby refluxing for 1.5 hours
  2. customwas returned to room temperature, to the mixture
  3. additionwas slowly added dropwise a solution
  4. customprepared
  5. customwas returned to room temperature
  6. customthe reaction
  7. extractionrepeatedly extracted with ethyl acetate
  8. washThe ethyl acetate layer was sufficiently washed with water
  9. customdried
  10. additionby adding anhydrous sodium sulfate
  11. customThe solvent was removed by distillation under reduced pressure
  12. customthe resulting solid was recrystallized from methylene chloride

출처 및 근거

ORD 기록
ord-314b0b1b98fc45a1b20a8bf062c2018f
출처 데이터셋
uspto-grants-1993_02
특허 번호
US05183934

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