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2-Iodo-5-trifluoromethylpyridine

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2-Iodo-5-trifluoromethylpyridine Basic information

Product Name:
2-Iodo-5-trifluoromethylpyridine
Synonyms:
  • 2-Iodo-5-(Trifluoromethyl)Pyri
  • 2-Iodo-5-trifluoromethylpyridine
  • 2-Iodo-5-(trifluoromethyl)pyridine
  • 5-(trifluoromethyl)-2-iodopyridine
  • Pyridine,2-iodo-5-(trifluoroMethyl)-
  • 6-Iodo-alpha,alpha,alpha-trifluoro-3-picoline
  • 2-Iodo-5-(trifluoromethyl)pyridine 98%
  • 2-Iodo-5-trifluoromethylpyridine ISO 9001:2015 REACH
CAS:
100366-75-4
MF:
C6H3F3IN
MW:
272.99
Product Categories:
  • Fluorine series
  • blocks
  • Iodides
  • Pyridines
Mol File:
100366-75-4.mol
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2-Iodo-5-trifluoromethylpyridine Chemical Properties

Melting point:
82-83 °C(Solv: hexane (110-54-3))
Boiling point:
215.7±40.0 °C(Predicted)
Density 
1.974±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
solid
pka
-0.58±0.10(Predicted)
color 
Off-white
Sensitive 
Light Sensitive
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Safety Information

Hazard Codes 
Xi,T
Risk Statements 
25
Safety Statements 
45
RIDADR 
2811
WGK Germany 
3
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2933399990
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2-Iodo-5-trifluoromethylpyridine Usage And Synthesis

Application

5-Trifluoromethyl-2-iodopyridine is a pyridine compound. Due to the electron-deficient nature of the pyridine ring, the iodine atom in its structure can undergo deiodination under the attack of strong nucleophiles. It can also undergo cross-coupling reactions with aryl halides catalyzed by metallic copper. Furthermore, this substance can undergo deiodination cyanation with aryl iodine in the presence of copper cyano, and can be used in the synthesis of pyridine cyanides.

Synthesis

52334-81-3

75-36-5

100366-75-4

a) Synthesis of 2-iodo-5-trifluoromethylpyridine: Sodium iodide (43.3 g, 289.1 mmol) was added to a solution of 2-chloro-5-trifluoromethylpyridine (15.0 g, 82.6 mmol) in acetonitrile (400 mL), and the reaction mixture was stirred at 88 °C until the sodium iodide was completely dissolved. Subsequently, acetyl chloride (8.8 mL, 12.3 mmol) was slowly added dropwise to the solution and precipitation was observed. The reaction mixture was refluxed for 24 hours, cooled and concentrated to give an oil. The oil was dissolved in dichloromethane, washed sequentially with 10% sodium thiosulfate solution, 10% sodium carbonate solution and saturated saline, dried over anhydrous magnesium sulfate, filtered and concentrated. The residue was purified by column chromatography using dichloromethane as eluent to give 10.9 g (48.4% yield) of light yellow target product.1H NMR (CDCl3): δ 8.68 (s, 1H), 7.88 (m, 1H), 7.49 (d, J = 9.9 Hz, 1H).

References

[1] Patent: US2003/45546, 2003, A1

2-Iodo-5-trifluoromethylpyridineSupplier

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