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5-Bromo-2-(trifluoromethyl)aniline

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5-Bromo-2-(trifluoromethyl)aniline Basic information

Product Name:
5-Bromo-2-(trifluoromethyl)aniline
Synonyms:
  • 5-BROMO-O-(TRIFLUOROMETHYL)ANILINE
  • 5-BROMO-2-(TRIFLUOROMETHYL)ANILINE
  • 2-Amino-4-bromobenzotrifluoride 98%
  • 5-Bromo-2-(trifluoromethyl)aniline, 5-Bromo-alpha,alpha,alpha-trifluoro-o-toluidine
  • 2-AMino-4-broMobenzotrifluoride
  • 5-Bromo-2-(trifluoro
  • 5-BroMo-2-trifluoroMethyl-phenylaMine
  • Benzenamine, 5-bromo-2-(trifluoromethyl)-
CAS:
703-91-3
MF:
C7H5BrF3N
MW:
240.02
Mol File:
703-91-3.mol
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5-Bromo-2-(trifluoromethyl)aniline Chemical Properties

Boiling point:
84-86 °C(Press: 5 Torr)
Density 
1.712 g/cm3(Temp: 25 °C)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
0.39±0.10(Predicted)
Appearance
Pale purple to purple Solid
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Safety Information

HS Code 
2921430090
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5-Bromo-2-(trifluoromethyl)aniline Usage And Synthesis

Synthesis

251115-21-6

703-91-3

General procedure for the synthesis of 5-bromo-2-(trifluoromethyl)aniline from 4-bromo-2-nitro-trifluoromethylbenzene: to a suspension of 4-bromo-2-nitro-1-(trifluoromethyl)benzene (4.0 g, 14.9 mmol) in ethanol (230 mL), THF (85 mL), and water (40 mL), ammonium chloride (1.0 g, 18.8 mmol) and iron powder (5.06 g, 90 mmol). The reaction mixture was heated at 80 °C for 1 h and the progress of the reaction was monitored by thin layer chromatography (TLC). After complete consumption of starting materials, the reaction mixture was filtered while hot. The filtrate was concentrated under reduced pressure and the crude product was dissolved in ethyl acetate (100 mL) and washed with water (3 x 50 mL). The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 5-bromo-2-(trifluoromethyl)aniline as a solid (3.2 g, 90% yield).

References

[1] Patent: WO2010/91310, 2010, A1. Location in patent: Page/Page column 100
[2] Patent: WO2014/149164, 2014, A1. Location in patent: Paragraph 00763; 00895

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