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2-Bromo-4-iodoanisole

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2-Bromo-4-iodoanisole Basic information

Product Name:
2-Bromo-4-iodoanisole
Synonyms:
  • 2-Bromo-4-iodoanisole
  • 2-Bromo-4-iodo-1-methoxybenzene, 2-Bromo-4-iodophenyl methyl ether
  • Benzene, 2-bromo-4-iodo-1-methoxy-
  • 2-bromo-4-iodobenzene methyl ether
CAS:
182056-39-9
MF:
C7H6BrIO
MW:
312.93
Product Categories:
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Bromine Compounds
  • Iodine Compounds
Mol File:
182056-39-9.mol
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2-Bromo-4-iodoanisole Chemical Properties

Melting point:
80-82 °C(Solv: hexane (110-54-3); toluene (108-88-3))
Boiling point:
285.1±30.0 °C(Predicted)
Density 
2.062±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
crystals
color 
Off white to faint peach
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Safety Information

HS Code 
2909309090
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2-Bromo-4-iodoanisole Usage And Synthesis

Uses

2-Bromo-4-iodoanisole is an electrophilic intermediate used in organic synthesis.

Preparation

2-Bromo-4-iodoanisole is synthetically prepared by regioselective halogenations of 4-iodoanisole.

Synthesis

578-57-4

182056-39-9

The general procedure for the synthesis of 2-bromo-4-iodo-1-methoxybenzene from 2-bromoanisole was as follows: to a stirred solution of 2-bromoanisole (1 mmol) in dichloromethane (CH2Cl2) or 1,2-dichloroethane ((CH2Cl)2) (0.1 M) was added sequentially Ph3PAuNTf2 (0.025 mmol, 19 mg; if using the 2:1 complex of Ph3PAuNTf2 with toluene) and N-iodosuccinimide (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 gradient elutions of hexane and ethyl acetate (EtOAc) to give pure 2-bromo-4-iodo-1-methoxybenzene.

References

[1] Synlett, 2014, vol. 25, # 3, p. 399 - 402
[2] Synthetic Communications, 2007, vol. 37, # 8, p. 1259 - 1265
[3] Canadian Journal of Chemistry, 2005, vol. 83, # 10, p. 1808 - 1811
[4] Tetrahedron Letters, 2004, vol. 45, # 43, p. 8015 - 8018

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