Hydrochloric Acid → 5-Amino-2-methoxybenzotrifluoride

HRID 649830

반응식

HRID 649830 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-])=O)=[CH:5][C:4]=1[C:12]([F:15])([F:14])[F:13].Cl>C(O)C.O.[Fe]>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[CH:5][C:4]=1[C:12]([F:13])([F:14])[F:15]

참가 물질

6

실험 절차

A suspension of 4-methoxy-3-trifluoromethyl-nitrobenzene (2.2 g) and iron powder (1.68 g) in ethanol (35 mL) and water (15 mL) is treated with a solution of concentrated hydrochloric acid (0.42 mL) in ethanol (6 mL) and water (3 mL) and the mixture is heated to reflux for approximately 1 hour. The mixture is then cooled, filtered, and concentrated under reduced pressure. The resulting oil is dissolved in ethyl acetate and extracted three times with 5% aqueous hydrochloric acid. The pooled acidic extracts are then cooled in an ice bath and basified with solid potassium carbonate, then extracted with ethyl acetate. These organic extracts are washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, concentrated under reduced pressure, then passed through a short column of silica gel (ethyl acetate is used as the eluant) to provide the desired compound as an amber oil.

후처리

  1. temperaturethe mixture is heated
  2. temperatureto reflux for approximately 1 hour
  3. temperatureThe mixture is then cooled
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. dissolutionThe resulting oil is dissolved in ethyl acetate
  7. extractionextracted three times with 5% aqueous hydrochloric acid
  8. temperatureThe pooled acidic extracts are then cooled in an ice bath
  9. extractionextracted with ethyl acetate
  10. washThese organic extracts are washed with saturated aqueous sodium chloride
  11. dry with materialdried over anhydrous sodium sulfate
  12. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-4d1a94bb82564ed5bd47bbf9850f6094
출처 데이터셋
uspto-grants-2001_08
특허 번호
US06271236B1

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