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3-CHLORO-5-FLUOROPHENYLACETONITRILE

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3-CHLORO-5-FLUOROPHENYLACETONITRILE Basic information

Product Name:
3-CHLORO-5-FLUOROPHENYLACETONITRILE
Synonyms:
  • 3-CHLORO-5-FLUOROPHENYLACETONITRILE
  • 3-CHLORO-5-FLUOROBENZYL CYANIDE
  • SALOR-INT L301035-1EA
  • 3-Chloro-5-fluorophenyl acetonitrile,98%
  • 3-Chloro-5-fluorophenylacetoni
  • 2-(3-Chloro-5-fluorophenyl)acetonitrile
  • Benzeneacetonitrile, 3-chloro-5-fluoro-
  • 3-Chloro-5-fluorophenylacetonitrile,97%
CAS:
493038-93-0
MF:
C8H5ClFN
MW:
169.58
Product Categories:
  • Fluorine series
  • Nitrile
Mol File:
493038-93-0.mol
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3-CHLORO-5-FLUOROPHENYLACETONITRILE Chemical Properties

Boiling point:
244.7±25.0 °C(Predicted)
Density 
1.286±0.06 g/cm3(Predicted)
refractive index 
1.523-1.525
storage temp. 
Sealed in dry,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow to Light orange
Water Solubility 
Not miscible or difficult to mix with water.
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Safety Information

Hazard Codes 
Xn,T
Risk Statements 
36/37/38-20/21/22-36/37/39
Safety Statements 
36/37/39-26
RIDADR 
UN 3276 6.1/PG III
Hazard Note 
Toxic
HazardClass 
6.1
PackingGroup 
III
HS Code 
2926907090

MSDS

  • Language:English Provider:ACROS
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3-CHLORO-5-FLUOROPHENYLACETONITRILE Usage And Synthesis

Chemical Properties

clear yellow liquid

Uses

It is employed as a intermediates for pharmaceutical.

Synthesis

773837-37-9

493024-39-8

493038-93-0

3-Chloro-5-fluorobenzyl bromide (58.23 g, 260 mmol) and acetic acid (5.35 mL, 93.6 mmol) were dissolved in toluene (260 mL). Aqueous sodium cyanide (195 mL, 48.57 g, 990 mmol) and tributylbenzyl ammonium chloride (5.68 g, 18.2 mmol) were added slowly and dropwise with stirring. The reaction mixture was stirred continuously at room temperature for 4 hours. After completion of the reaction, the organic layer was separated and washed sequentially with deionized water (200 mL) and saturated sodium chloride solution (200 mL). The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. The crude product obtained was purified by basic silica gel column chromatography using hexane-ethyl acetate (4:1, v/v) as eluent to give 3-chloro-5-fluorophenylacetonitrile (44.89 g, 100% yield) as a brown oil. The structure of the product was confirmed by 1H NMR (300 MHz, CDCl3): δ 3.74 (2H, s), 6.99 (1H, d, J = 8.7 Hz), 7.05-7.13 (1H, m), 7.15 (1H, s).

References

[1] Patent: EP2530078, 2012, A1. Location in patent: Page/Page column 118

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