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4-CYANO-2-FLUOROBENZALDEHYDE

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4-CYANO-2-FLUOROBENZALDEHYDE Basic information

Product Name:
4-CYANO-2-FLUOROBENZALDEHYDE
Synonyms:
  • 4-CYANO-2-FLUOROBENZALDEHYDE
  • 2-FLUORO-4-CYANOBENZALDEHYDE
  • Benzonitrile, 3-fluoro-4-formyl- (9CI)
  • Benzonitrile, 3-fluoro-4-formyl-
  • 3-Fluoro-4-formylbenzonitrile 99%
  • 4-Cyano-2-fluorobenzaldehyde, 98%+
  • 4-CYANO-2-FLUOROBENZALDEHYDE ISO 9001:2015 REACH
CAS:
105942-10-7
MF:
C8H4FNO
MW:
149.12
Product Categories:
  • Fluorine series
  • Drug Intermediates
  • HALIDE
  • ALDEHYDE
Mol File:
105942-10-7.mol
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4-CYANO-2-FLUOROBENZALDEHYDE Chemical Properties

Melting point:
73.2-75
Boiling point:
275.8±25.0 °C(Predicted)
Density 
1.25±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
crystalline solid
color 
Light brown
CAS DataBase Reference
105942-10-7(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2926907090
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4-CYANO-2-FLUOROBENZALDEHYDE Usage And Synthesis

Synthesis

133059-44-6

97674-02-7

105942-10-7

a) Preparation of the intermediate: 4-bromo-3-fluorobenzonitrile (6.0 g, 30.00 mmol) and tributyl(1-ethoxyvinyl)tin (11.2 mL, 33.00 mmol) were dissolved in toluene (100 mL) under nitrogen protection and stirred at room temperature. Dichlorobis(triphenylphosphine)palladium(II) (0.72 g, 1.03 mmol) was then added and stirring continued at room temperature. The reaction mixture was heated to reflux temperature and stirred overnight. After the reaction was completed, it was cooled to room temperature and 2 M potassium fluoride solution (50 mL) was slowly added and stirred for 30 minutes. Next, 6 M hydrochloric acid solution (100 mL) was added, heated to 70°C and stirred for 2 hours. The insoluble material was removed by filtration and the filtrate was extracted with ethyl acetate (3 × 80 mL). The organic layers were combined, washed with saturated brine, dried over anhydrous magnesium sulfate, filtered and the solvent was concentrated under reduced pressure. Intermediate 14 was obtained in a yield of 4.3 g, 88% yield.

References

[1] Patent: WO2011/154298, 2011, A1. Location in patent: Page/Page column 36-37

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