Basic information Safety Supplier Related

2-BROMO-5-IODOANISOLE

Basic information Safety Supplier Related

2-BROMO-5-IODOANISOLE Basic information

Product Name:
2-BROMO-5-IODOANISOLE
Synonyms:
  • 2-BROMO-5-IODOANISOLE
  • Benzene, 1-broMo-4-iodo-2-Methoxy-
  • 1-Bromo-4-iodo-2-methoxybenzene, 2-Bromo-5-iodophenyl methyl ether
  • 2-BroMo-5-iodophenyl Methyl ether
  • 2-Bromo-5-iodoanisole 98%
  • 2-bromo-5-iodophenyl ether
  • 2-iodine-5-bromophenyl ether
CAS:
755027-18-0
MF:
C7H6BrIO
MW:
312.93
Product Categories:
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Bromine Compounds
  • Iodine Compounds
  • Aromatic Halides (substituted)
Mol File:
755027-18-0.mol
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2-BROMO-5-IODOANISOLE Chemical Properties

Boiling point:
293.7±20.0 °C(Predicted)
Density 
2.062
storage temp. 
Keep in dark place,Sealed in dry,2-8°C
form 
crystalline needles
color 
Faint yellow
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2909309090
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2-BROMO-5-IODOANISOLE Usage And Synthesis

Synthesis

19056-40-7

755027-18-0

4-Bromo-3-methoxyaniline (102 mg, 0.50 mmol) was used as starting material and dissolved in concentrated hydrochloric acid (10 mL) at 0 °C. Subsequently, an aqueous solution of sodium nitrite (NaNO2, 45 mg, 0.65 mmol) (5 mL) was slowly added, the reaction temperature was maintained at 0 °C and the reaction was stirred for 1 hour. Next, an aqueous solution of potassium iodide (KI, 249 mg, 1.5 mmol) (5 mL) was added, and the reaction mixture was gradually warmed to room temperature and stirred overnight. After completion of the reaction, the product was extracted with ethyl acetate. The organic phase was washed sequentially with water and 10% sodium thiosulfate (Na2S2O3) solution, dried over anhydrous magnesium sulfate (MgSO4), filtered and concentrated to give 147 mg of 2-bromo-5-iodoanisole in 94% yield. The product was analyzed by mass spectrometry (ESI), m/e 332 (M + 20)+; nuclear magnetic resonance hydrogen spectrum (1H NMR, 300 MHz, DMSO-d6) δ 7.39 (d, J = 1.87 Hz, 1H), 7.34 (d, J = 8.11 Hz, 1H), 7.24 (dd, J = 8.11, 1.87 Hz, 1H), 3.86 (s 3H).

References

[1] European Journal of Organic Chemistry, 2018, vol. 2018, # 38, p. 5312 - 5322
[2] Patent: WO2004/76424, 2004, A1. Location in patent: Page 79
[3] Journal of the American Chemical Society, 2018,
[4] Patent: WO2007/37187, 2007, A1. Location in patent: Page/Page column 127-128
[5] Patent: WO2008/57208, 2008, A2. Location in patent: Page/Page column 50

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