Basic information Safety Supplier Related

5-IODO-2-METHOXYTOLUENE

Basic information Safety Supplier Related

5-IODO-2-METHOXYTOLUENE Basic information

Product Name:
5-IODO-2-METHOXYTOLUENE
Synonyms:
  • 5-IODO-2-METHOXYTOLUENE
  • 4-IODO-2-METHYLANISOLE
  • 5-IODO-2-METHYLANISOLE
  • 4-Iodo-1-Methoxy-2-Methylbenzene
  • Benzene, 4-iodo-1-methoxy-2-methyl-
CAS:
75581-11-2
MF:
C8H9IO
MW:
248.06
Product Categories:
  • Aromatic Ethers
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Iodine Compounds
Mol File:
75581-11-2.mol
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5-IODO-2-METHOXYTOLUENE Chemical Properties

Melting point:
75-76 °C(Solv: acetic acid (64-19-7))
Boiling point:
247.7±28.0 °C(Predicted)
Density 
1.634±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
Appearance
Off-white to gray Solid
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
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5-IODO-2-METHOXYTOLUENE Usage And Synthesis

Synthesis Reference(s)

Tetrahedron Letters, 37, p. 4081, 1996 DOI: 10.1016/0040-4039(96)00738-1

Synthesis

578-58-5

75581-11-2

The general procedure for the synthesis of 4-iodo-2-methylanisole from 2-methylanisole is as follows: to a stirred solution of 2-methylanisole (1 mmol) in dichloromethane (CH2Cl2) or 1,2-dichloroethane ((CH2Cl)2) (0.1 M), triphenylphosphorane-gold bis(trifluoromethylsulfonyl)imide (Ph3PAuNTf2) (0.025 mmol , 19 mg; if toluene-coordinated Ph3PAuNTf2 complex was used, the ratio was 2:1), followed by the addition of N-iodosuccinimide (NIS) (1.1 mmol, 248 mg). The reaction mixture was stirred at room temperature or reacted under reflux conditions until complete conversion of the feedstock was confirmed by thin layer chromatography (TLC) monitoring. Upon completion of the reaction, the solvent was evaporated under reduced pressure and the resulting crude product was purified by fast column chromatography using different ratios of hexane and ethyl acetate (EtOAc) as eluents to finally obtain pure 4-iodo-2-methylanisole.

References

[1] Synthetic Communications, 2003, vol. 33, # 8, p. 1319 - 1323
[2] Chemistry Letters, 1988, # 5, p. 795 - 798
[3] Synlett, 2014, vol. 25, # 3, p. 399 - 402
[4] Tetrahedron Letters, 1996, vol. 37, # 23, p. 4081 - 4084
[5] Journal of Organic Chemistry, 2006, vol. 71, # 11, p. 4349 - 4352

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