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1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE

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1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE Basic information

Product Name:
1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE
Synonyms:
  • 1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE
  • 1-Bromo-2,3-difluoro-4-methoxybenzene
  • 4-Bromo-2,3-difluoroanisole
  • 4-Bromo-2,3-difluoroanisole 98%
  • 4-Bromo-2,3-difluoroanisole98%
  • Benzene, 1-bromo-2,3-difluoro-4-methoxy-
  • 1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE ISO 9001:2015 REACH
CAS:
406482-22-2
MF:
C7H5BrF2O
MW:
223.01
EINECS:
000-000-0
Product Categories:
  • blocks
  • Bromides
Mol File:
406482-22-2.mol
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1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE Chemical Properties

Melting point:
56-58°
Boiling point:
203.2±35.0 °C(Predicted)
Density 
1.615
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
Appearance
White to off-white Solid
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2909309090
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1-BROMO-4-METHOXY-2,3-DIFLUOROBENZENE Usage And Synthesis

Synthesis

144292-32-0

74-88-4

406482-22-2

General procedure: iodomethane (1.56 mL, 25.1 mmol, 1.5 eq.) was slowly added dropwise to a suspension of 2,3-difluoro-4-bromophenol (3.5 g, 16.7 mmol) and potassium carbonate (2.77 g, 20.0 mmol, 1.2 eq.) in N,N-dimethylformamide (30 mL). The reaction mixture was stirred at room temperature for 3 days. After completion of the reaction, the insoluble precipitate was removed by filtration. The filtrate was concentrated to dryness under reduced pressure. Dichloromethane and water were added to the residue and the product was extracted with dichloromethane. The organic phases were combined, dried over anhydrous magnesium sulfate and subsequently concentrated under reduced pressure to afford 4-bromo-2,3-difluoroanisole as a white crystalline solid (3.8 g, quantitative yield).

References

[1] Patent: WO2012/175991, 2012, A1. Location in patent: Page/Page column 78

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