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2-Methoxy-5-Iodopyridine

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2-Methoxy-5-Iodopyridine Basic information

Product Name:
2-Methoxy-5-Iodopyridine
Synonyms:
  • 2-Methoxy-5-Iodopyridine
  • 5-Iodo-2-methoxypyridine 98%
  • 5-Iodo-2-methoxypyridine>
  • Pyridine, 5-iodo-2-methoxy-
  • 5-lodo-2-methoxypyridine
CAS:
13472-61-2
MF:
C6H6INO
MW:
235.02
Product Categories:
  • Pyridine
Mol File:
13472-61-2.mol
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2-Methoxy-5-Iodopyridine Chemical Properties

Boiling point:
237℃
Density 
1.825
refractive index 
1.6060 to 1.6100
Flash point:
97℃
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
form 
Liquid
pka
1.38±0.10(Predicted)
color 
Clear colorless to pale yellow
Sensitive 
Light Sensitive
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Safety Information

HS Code 
29333990
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2-Methoxy-5-Iodopyridine Usage And Synthesis

Synthesis

13472-85-0

13472-61-2

The general procedure for the synthesis of 5-bromo-2-methoxypyridine from 5-bromo-2-methoxypyridine was as follows: n-butyllithium (1.5 M in hexane solution, 4.98 mL, 7.47 mmol) was slowly added to a solution of isopropylmagnesium chloride (1.61 M in THF, 4.64 mL, 7.47 mmol) in THF (20 mL) under ice bath cooling conditions. The reaction mixture was stirred for 5 min to form a yellow solution after which 5-bromo-2-methoxypyridine (1.405 g, 0.98 mL, 7.10 mmol, 95%) was added. The resulting solution was continued to be stirred at 0 °C for 45 min. Molecular iodine (3.79 g, 14.94 mmol) was then added and the reaction mixture was stirred at 0°C for 30 minutes and then at room temperature for 1 hour. Upon completion of the reaction, the reaction was quenched by the addition of aqueous ammonium chloride (5 mL) and the organic and aqueous phases were separated. The aqueous phase was extracted with ethyl acetate (2 x 75 mL), and the combined organic layers were dried with magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (ethyl acetate-heptane, 5-80%) to afford the target product 5-iodo-2-methoxypyridine.

References

[1] Synthesis, 2012, vol. 44, # 5, p. 735 - 746
[2] Synthesis (Germany), 2015, vol. 47, # 20, p. 3231 - 3240
[3] Journal of the American Chemical Society, 2015, vol. 137, # 33, p. 10480 - 10483

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