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2-Amino-5-trifluoromethylbenzonitrile

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2-Amino-5-trifluoromethylbenzonitrile Basic information

Product Name:
2-Amino-5-trifluoromethylbenzonitrile
Synonyms:
  • 2-Amino-5-trifluoromethylbenzonitrile
  • 4-Amino-3-cyanobenzotrifluoride
  • Benzonitrile, 2-aMino-5-(trifluoroMethyl)-
  • 4-Amino-3-cyanobenzotrifluoride, 2-Cyano-4-(trifluoromethyl)aniline
  • 0/5/26
CAS:
6526-08-5
MF:
C8H5F3N2
MW:
186.13
Product Categories:
  • Fluorine series
  • Benzotrifluoride Series
Mol File:
6526-08-5.mol
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2-Amino-5-trifluoromethylbenzonitrile Chemical Properties

Melting point:
72-74 °C(Solv: benzene (71-43-2))
Boiling point:
95-115 C
Density 
1.37±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
-0.02±0.10(Predicted)
form 
crystalline powder
color 
Faint lemon
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Safety Information

Hazard Codes 
T
HS Code 
2926907090
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2-Amino-5-trifluoromethylbenzonitrile Usage And Synthesis

Synthesis

544-92-3

57946-63-1

6526-08-5

A reaction was carried out with cuprous cyanide (2.24 g, 25.00 mmol) and 2-bromo-4-(trifluoromethyl)aniline (5.0 g, 20.83 mmol) in N-methyl-2-pyrrolidone (20 mL) heated at 195 °C for 4 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate (100 mL) and washed twice with 28% aqueous ammonium hydroxide solution, twice with saturated aqueous sodium chloride solution (brine), and twice with water, in that order. The organic layer was separated, dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The resulting residue was purified by fast chromatography using hexane as the starting eluent and gradually increasing the proportion of ethyl acetate to a gradient elution of 30% hexane-70% ethyl acetate, resulting in 2-amino-5-trifluoromethylbenzonitrile (1.821 g, 9.78 mmol, 47% yield) as a green amorphous solid. Mass spectrum (m/e): 187 (M + 1).

References

[1] Patent: WO2004/14895, 2004, A1. Location in patent: Page 68

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