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4-Fluoro-3-methoxybenzonitrile

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4-Fluoro-3-methoxybenzonitrile Basic information

Product Name:
4-Fluoro-3-methoxybenzonitrile
Synonyms:
  • BUTTPARK 22\01-64
  • 4-FLUORO-3-METHOXYBENZONITRILE
  • Benzonitrile, 4-fluoro-3-methoxy- (9CI)
  • 4-Fluoro-3-methoxybenzonitrile 99%
  • 4-Fluoro-3-methoxybenzonitrile99%
  • 3-Methoxy-4-Fluorobenzonitrile
  • 5-Cyano-2-fluoroanisole, 5-Cyano-2-fluorophenyl methyl ether
  • 5-Cyano-2-fluoroanisole
CAS:
243128-37-2
MF:
C8H6FNO
MW:
151.14
EINECS:
607-355-6
Product Categories:
  • blocks
  • Carboxes
  • FluoroCompounds
  • Nitrile
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Fluorine Compounds
  • Nitriles
  • HALIDE
Mol File:
243128-37-2.mol
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4-Fluoro-3-methoxybenzonitrile Chemical Properties

Melting point:
109 °C
Boiling point:
96-98°C 1,5mm
Density 
1.18±0.1 g/cm3(Predicted)
Flash point:
96-98°C/1.5mm
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Toluene
form 
powder to crystal
color 
White to Light yellow to Light orange
BRN 
2965042
CAS DataBase Reference
243128-37-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T,Xi,Xn
Risk Statements 
20/21/22-36/37/38-22
Safety Statements 
26-36/37/39-36/37-9
RIDADR 
3439
Hazard Note 
Toxic
HazardClass 
6.1
PackingGroup 
III
HS Code 
29269090

MSDS

  • Language:English Provider:ALFA
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4-Fluoro-3-methoxybenzonitrile Usage And Synthesis

Chemical Properties

White powder

Synthesis

946713-86-6

57-13-6

243128-37-2

Cu(TFA)2 (20 mmol) was added to a pressure-sealed tube containing 0.75 mL of DMSO with 4-fluoro-3-methoxyphenylacetic acid (0.5 mmol) and urea (1.5 mmol). The reaction system was oxygenated and stirred at 130 °C for about 20 h. The reaction process was monitored by TLC and GC (the exact reaction time was determined based on GC and TLC monitoring results). Upon completion of the reaction, the reaction was cooled to room temperature. To the reaction mixture, 20 mL of ethyl acetate was added and washed sequentially with NaHCO3 solution (20 mL x 2) and water. The organic phases were combined and dried over anhydrous sodium sulfate. The aqueous phase was then extracted with ethyl acetate (20 mL x 2) and all organic phases were combined. The solvent was removed by rotary evaporator to obtain the crude product. The crude product was purified by silica gel column chromatography with the eluent ratio of ethyl acetate:petroleum ether=50:1. 4-fluoro-3-methoxybenzonitrile was finally obtained in 84% yield.

References

[1] Patent: CN103772236, 2016, B. Location in patent: Paragraph 0021; 0022; 0023; 0054; 0055; 0056; 0057

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