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2-Bromo-3-fluoronitrobenzene

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2-Bromo-3-fluoronitrobenzene Basic information

Product Name:
2-Bromo-3-fluoronitrobenzene
Synonyms:
  • 2-BROMO-3-FLUORONITROBENZENE
  • 2-broMo-3-fluorobroMobezene
  • 2-Bromo-1-fluoro-3-nitrobenzene
  • Benzene, 2-bromo-1-fluoro-3-nitro-
  • 2-Bromo-3-fluoronitrobenzene ISO 9001:2015 REACH
  • 1-Bromo-2-fluoro-6-nitrobenzene
CAS:
59255-94-6
MF:
C6H3BrFNO2
MW:
220
EINECS:
1533716-785-6
Product Categories:
  • blocks
  • Bromides
  • FluoroCompounds
  • NitroCompounds
Mol File:
59255-94-6.mol
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2-Bromo-3-fluoronitrobenzene Chemical Properties

Melting point:
42.0-44.0 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
Boiling point:
222.3±20.0 °C(Predicted)
Density 
1.808±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
solid
color 
yellow
CAS DataBase Reference
59255-94-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T
HazardClass 
IRRITANT
HS Code 
2904990090
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2-Bromo-3-fluoronitrobenzene Usage And Synthesis

Synthesis

Preparation method of 2-bromo-3-fluoronitrobenzene: Add 21.6g (0.1mol) 2-bromo-3-nitroaniline, 12.5ml (0.15mol) concentrated hydrochloric acid, and 12.5ml water into a reaction bottle, and reduce the temperature to 15°C; dissolve 8.3g (0.12mol) sodium nitrite in 14.5ml water and slowly add dropwise to the above system, then add 11.4g (0.13mol) fluoroboric acid, keep warm at 15°C and stir for 2 hours, track the reaction by HPLC until the reaction of 2-bromo-3-nitroaniline is complete; filter, rinse the filter cake with methanol, and dry to obtain 25.8g of intermediate IV. Add 30 ml of toluene to the reaction flask, heat to 100 ° C, slowly add 10 g (31.7 mmol) of intermediate IV, keep warm and stir for 1 hour, track the reaction by HPLC until the intermediate IV reacts completely: concentrate, recrystallize from ethyl acetate and n-hexane to obtain 5.7 g of 2-Bromo-3-fluoronitrobenzene, with a molar yield of 83%.

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