Basic information Uses Safety Supplier Related
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2-AMINO-4-FLUOROBENZONITRILE

Basic information Uses Safety Supplier Related

2-AMINO-4-FLUOROBENZONITRILE Basic information

Product Name:
2-AMINO-4-FLUOROBENZONITRILE
Synonyms:
  • 4-Fluoroanthranilonitrile, 2-Cyano-5-fluoroaniline
  • Amino-4-fluorobenzonitrile
  • 2-Amino-4-fluorobenzonitrile
  • Benzonitrile, 2-amino-4-fluoro-
  • 4-Fluoroanthranilonitrile
CAS:
80517-22-2
MF:
C7H5FN2
MW:
136.13
Product Categories:
  • Phenyls & Phenyl-Het
Mol File:
80517-22-2.mol
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2-AMINO-4-FLUOROBENZONITRILE Chemical Properties

Melting point:
102.2 °C (decomp)
Boiling point:
284.7±25.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
crystals
pka
0.80±0.10(Predicted)
color 
Light purple
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Safety Information

HazardClass 
TOXIC
HS Code 
2926907090
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2-AMINO-4-FLUOROBENZONITRILE Usage And Synthesis

Uses

2-Amino-4-fluorobenzonitrile is a useful research chemical for organic synthesis and other chemical processes.

Synthesis

3939-09-1

80517-22-2

53312-80-4

Using 2,4-difluorobenzonitrile (2.78 g, 20 mmol) and 3,4,5-trimethoxybenzylamine (3.94 g, 20 mmol) as raw material, the two were mixed and heated at 140 °C for 40 min. After completion of the reaction, the mixture was cooled to room temperature and subsequently dissolved in trifluoroacetic acid (TFA, 20 mL) and stirred at room temperature overnight. Afterwards, the mixture was concentrated using a rotary evaporator and subsequently partitioned between 1N NaOH solution (~100 mL, adjusted to alkaline) and ethyl acetate (100 mL). After separation of the organic layer, the aqueous layer was extracted with additional ethyl acetate (100 mL). All organic layers were combined, washed with brine (50 mL), dried over anhydrous magnesium sulfate (MgSO4) and concentrated to give an oil. Separation of the mixture by column chromatography (eluent: 10% to 40% hexane solution of ethyl acetate) gave two well separated isomeric products. Further concentration gave 4-amino-2-fluorobenzonitrile (1.07 g, 39% yield) as a white solid. The structure of the product was confirmed by LC/MS (m/z = 177.8, corresponding to the determination of [M+H]+ in acetonitrile).

References

[1] Patent: US2008/76813, 2008, A1. Location in patent: Page/Page column 28

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