Acetic Acid → 2-Bromo-5-chloro-4-(trifluoromethyl)aniline

HRID 1670738Notes

Reaction equation

HRID 1670738 reaction equation
C(O)(=O)C.O.[Br:6][C:7]1[C:8]([N+:18]([O-])=O)=[CH:9][C:10]([Cl:17])=[C:11]([C:13]([F:16])([F:15])[F:14])[CH:12]=1.C(OCC)(=O)C>O1CCOCC1>[Br:6][C:7]1[CH:12]=[C:11]([C:13]([F:14])([F:16])[F:15])[C:10]([Cl:17])=[CH:9][C:8]=1[NH2:18]

Participants

6

Conditions

Temperature
60 °C

Procedure

A mixture of reduced iron (17.7 g), acetic acid (290 ml) and water (145 ml) was stirred with heating at 60° C. for 15 min, 5-bromo-2-chloro-4-nitrobenzotrifluoride (17.7 g) dissolved in 1,4-dioxane (100 ml) was added thereto, and the mixture was stirred with heating at 60° C. for 30 min. The reaction mixture was ice-cooled, ethyl acetate (700 ml) was added and the mixture was stirred at room temperature, The reaction mixture was filtered through a celite (trademark) filter. The filtrate was washed three times with a 1N aqueous sodium hydroxide solution and then with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give 2-bromo-5-chloro-4-(trifluoromethyl)aniline (17.1 g, yield 100%).

Workup

  1. additionwas added
  2. stirringthe mixture was stirred
  3. temperaturewith heating at 60° C. for 30 min
  4. temperaturecooled
  5. stirringthe mixture was stirred at room temperature
  6. filtrationThe reaction mixture was filtered through a celite (trademark)
  7. filtrationfilter
  8. washThe filtrate was washed three times with a 1N aqueous sodium hydroxide solution
  9. dry with materialwith saturated brine, and dried over anhydrous sodium sulfate
  10. customThe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-43e193bc77b8493ca2c322b3fe39ca2a
Source dataset
uspto-grants-2011_08
Patent number
US07994196B2

Reaction notes

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