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3-IODO-4-METHOXY-PYRIDINE

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3-IODO-4-METHOXY-PYRIDINE Basic information

Product Name:
3-IODO-4-METHOXY-PYRIDINE
Synonyms:
  • 3-IODO-4-METHOXY-PYRIDINE
  • Pyridine, 3-iodo-4-methoxy-
CAS:
89640-55-1
MF:
C6H6INO
MW:
235.02
Mol File:
89640-55-1.mol
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3-IODO-4-METHOXY-PYRIDINE Chemical Properties

Melting point:
78 °C(Solv: ligroine (8032-32-4))
Boiling point:
271.2±25.0 °C(Predicted)
Density 
1.825±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
4.52±0.18(Predicted)
form 
solid
Appearance
White to yellow Solid
InChI
InChI=1S/C6H6INO/c1-9-6-2-3-8-4-5(6)7/h2-4H,1H3
InChIKey
WZAPSURIRLYQEJ-UHFFFAOYSA-N
SMILES
C1=NC=CC(OC)=C1I
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933399990
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3-IODO-4-METHOXY-PYRIDINE Usage And Synthesis

Synthesis

620-08-6

89640-55-1

The general procedure for the synthesis of 3-iodo-4-methoxypyridine from 4-methoxypyridine was as follows: n-butyllithium (ca. 1.6 M hexane solution, 1.5 mmol) was sequentially added to a stirred solution of 2,2,6,6-tetramethylpiperidine (0.25 mL, 1.5 mmol) in tetrahydrofuran (THF, 2-3 mL) at 0 °C. After 5 min, n-butyllithium (ca. 1.6 M hexane solution, 1.5 mmol) was added. ZnCl2TMEDA complex (0.13 g, 0.50 mmol). The reaction mixture was continued to be stirred at 0 °C for 15 min and then 4-methoxypyridine (1.0 mmol) was added at 0-10 °C. After the reaction mixture was stirred for 2 h at room temperature, a THF (4 mL) solution of iodine (I2, 0.38 g, 1.5 mmol) was added. After the mixture was stirred overnight, the reaction was quenched by the addition of saturated aqueous sodium thiosulfate (Na2S2O3) solution (4 mL) and extracted with ethyl acetate (AcOEt, 320 mL). The organic layers were combined, dried with anhydrous magnesium sulfate (MgSO4), filtered and concentrated under reduced pressure. Finally, the target product, 3-iodo-4-methoxypyridine, was purified by silica gel column chromatography (eluent given in the product specification).

References

[1] Tetrahedron, 2016, vol. 72, # 17, p. 2196 - 2205
[2] Tetrahedron, 1993, vol. 49, # 37, p. 8373 - 8380
[3] Tetrahedron Letters, 2011, vol. 52, # 36, p. 4590 - 4594
[4] Chemical Communications, 2014, vol. 50, # 85, p. 12859 - 12862
[5] Chemistry - A European Journal, 2013, vol. 19, # 24, p. 7944 - 7960

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