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2-Bromo-5-fluoroanisole

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2-Bromo-5-fluoroanisole Basic information

Product Name:
2-Bromo-5-fluoroanisole
Synonyms:
  • 2-BroMo-5-fluoroanisole, 95.0%(GC)
  • 1-Bromo-4-fluoro-2-methoxybenzene, 2-Bromo-5-fluorophenyl methyl ether
  • BUTTPARK 87\07-62
  • 2-BROMO-5-FLUOROANISOLE
  • 1-Bromo-4-fluoro-2-methoxybenzene
  • 2-Bromo-5-fluoroanisole98+%
  • 2-Bromo-5-fluoroanisole >
  • Benzene, 1-bromo-4-fluoro-2-methoxy-
CAS:
450-88-4
MF:
C7H6BrFO
MW:
205.02
Product Categories:
  • Anisole
Mol File:
450-88-4.mol
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2-Bromo-5-fluoroanisole Chemical Properties

Boiling point:
143-145 °C
Density 
1.5983
refractive index 
1.542
Flash point:
90 °C
storage temp. 
Inert atmosphere,Room Temperature
form 
clear liquid
color 
Colorless to Light yellow
InChIKey
KGYXKRGMSUHYCY-UHFFFAOYSA-N
CAS DataBase Reference
450-88-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
36/37/38-36-22
Safety Statements 
26-36/37/39
WGK Germany 
3
Hazard Note 
Harmful
HS Code 
29093090
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2-Bromo-5-fluoroanisole Usage And Synthesis

Chemical Properties

Colorless liquid to pale yellow liquid

Uses

2-Bromo-5-fluoroanisole is a halogenated anisole compound, the chemical reactivity of which is mainly concentrated on the bromine atom on its benzene ring. It can be used as an organic synthesis intermediate and a synthetic raw material for drug molecules. For example, literature reports that the substance can be used for the preparation of the drug molecule anacetrapib.

Synthesis

77-78-1

147460-41-1

450-88-4

a) A suspension of 2-bromo-5-fluorophenol (20.0 g, 104.7 mmol) and potassium carbonate (21.71 g, 157.1 mmol) was formed in acetone (200 mL). To this suspension dimethyl sulfate (10.90 mL, 115.2 mmol) was slowly added. The reaction mixture was stirred at 60 °C for 2 h. After completion of the reaction, it was cooled to room temperature and subsequently concentrated under reduced pressure to remove the solvent. The concentrated residue was dissolved in a mixture of ether (200 mL) and water (100 mL) to separate the organic phase. The organic phase was washed sequentially with 2N aqueous hydrochloric acid (50 mL) and saturated sodium bicarbonate solution (50 mL), and then dried with anhydrous magnesium sulfate. The dried organic phase was evaporated from the solvent under reduced pressure to give the light yellow oily product 2-bromo-5-fluoroanisole (21.46 g, 100% yield). The product was confirmed by NMR hydrogen spectrum (300 MHz, CDCl3): δ 7.45 (1H, dd, Ar-H), 6.70-6.55 (2H, m, Ar-H), 3.90 (3H, s, OCH3).

References

[1] Patent: WO2004/43903, 2004, A1. Location in patent: Page 29
[2] Patent: WO2004/43903, 2004, A1. Location in patent: Page 30
[3] Patent: WO2004/43904, 2004, A1. Location in patent: Page 28

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