Acetic Acid → 2-Bromo-5-chloro-4-(trifluoromethyl)aniline
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
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
- additionwas added
- stirringthe mixture was stirred
- temperaturewith heating at 60° C. for 30 min
- temperaturecooled
- stirringthe mixture was stirred at room temperature
- filtrationThe reaction mixture was filtered through a celite (trademark)
- filtrationfilter
- washThe filtrate was washed three times with a 1N aqueous sodium hydroxide solution
- dry with materialwith saturated brine, and dried over anhydrous sodium sulfate
- 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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