Basic information Safety Supplier Related

2-Amino-5-(1-methylethyl)benzonitrile

Basic information Safety Supplier Related

2-Amino-5-(1-methylethyl)benzonitrile Basic information

Product Name:
2-Amino-5-(1-methylethyl)benzonitrile
Synonyms:
  • Benzonitrile, 2-amino-5-(1-methylethyl)- (9CI)
  • Benzonitrile, 2-amino-5-(1-methylethyl)-
  • 2-Amino-5-(1-methylethyl)benzonitrile
  • 2-amino-5-isopropylbenzonitrile
  • 2-aMino-5-(propan-2-yl)benzonitrile
  • 2-amino-5-isopropylbenzonitrile - [AC78501]
CAS:
549488-76-8
MF:
C10H12N2
MW:
160.22
Product Categories:
  • ISOPROPYL
Mol File:
549488-76-8.mol
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2-Amino-5-(1-methylethyl)benzonitrile Chemical Properties

Boiling point:
285.8±33.0 °C(Predicted)
Density 
1.04±0.1 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
2.21±0.10(Predicted)
Appearance
Yellow to brown Solid
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2-Amino-5-(1-methylethyl)benzonitrile Usage And Synthesis

Synthesis

51605-97-1

544-92-3

549488-76-8

General procedure for the synthesis of 2-amino-5-(1-methylethyl)benzonitrile from 2-bromo-4-isopropylaniline and cuprous cyanide (I): a mixture of cuprous cyanide (I) (2.5 g, 28.02 mmol) and 2-bromo-4-isopropylaniline (5.0 g, 23.35 mmol) was heated in 1-methyl-2-pyrrolidinone (20 mL) to 195°C for for 4 hours. After completion of the reaction, the reaction mixture was diluted with ethyl acetate (100 mL) to give a dark solution. It was washed twice sequentially with 28% aqueous ammonium hydroxide, twice with saturated aqueous sodium chloride solution (brine) and twice with water. The organic layer was separated, dried with anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The product was purified by fast column chromatography with hexane as the starting eluent, and the gradient was increased to 20% ethyl acetate/80% hexane to give the orange oily product 2-amino-5-(1-methylethyl)benzonitrile (3.31 g, 20.66 mmol, 88% yield). Mass spectrum (m/z): 161 (M + 1).

References

[1] Patent: WO2004/14895, 2004, A1. Location in patent: Page 65-66
[2] Patent: WO2004/14895, 2004, A1. Location in patent: Page 62

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