Hydrochloric Acid → 5-Amino-2-methoxybenzotrifluoride

HRID 1532188Notes

Reaction equation

HRID 1532188 reaction equation
[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]

Participants

6

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-e3f3af6970c5411e8a6f161724edbb67
Source dataset
uspto-grants-2001_03
Patent number
US06201013B1

Reaction notes

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