2-Bromo-6-fluoronitrobenzene
2-Bromo-6-fluoronitrobenzene Basic information
- Product Name:
- 2-Bromo-6-fluoronitrobenzene
- Synonyms:
-
- 1-Bromo-3-fluoro-2-nitrobenzene
- 2-fluoro-6-bromonitrobenzene
- 2-Bromo-6-fluoronitrobenzene 97%
- 1-Bromo-3-fluoro-2-nitrobenzene >
- Benzene, 1-bromo-3-fluoro-2-nitro-
- 1-Bromo-3-fluoro-2-nitrobenzene ISO 9001:2015 REACH
- 3-bromo-3-fluoro-2-nitrobenzene
- 2-BROMO-6-FLUORONITROBENZENE
- CAS:
- 886762-70-5
- MF:
- C6H3BrFNO2
- MW:
- 220
- EINECS:
- 689-316-3
- Mol File:
- 886762-70-5.mol
2-Bromo-6-fluoronitrobenzene Chemical Properties
- Melting point:
- 36-37°C
- Boiling point:
- 232.0±20.0 °C(Predicted)
- Density
- 1.808±0.06 g/cm3(Predicted)
- Flash point:
- 87°
- storage temp.
- 2-8°C
- solubility
- soluble in Methanol
- form
- powder to lump
- color
- White to Orange to Green
- InChI
- InChI=1S/C6H3BrFNO2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H
- InChIKey
- VFPAOFBPEYCAAZ-UHFFFAOYSA-N
- SMILES
- C1(Br)=CC=CC(F)=C1[N+]([O-])=O
2-Bromo-6-fluoronitrobenzene Usage And Synthesis
Chemical Properties
light yellow crystalline powder
Uses
2-Bromo-6-fluoronitrobenzene is a hydrocarbon derivative, mainly used as an organic intermediate.
Reactions
The structure of 2-bromo-6-fluoronitrobenzene contains a nitro unit with high electron-withdrawing properties, which can easily undergo aromatic nucleophilic substitution reactions under the attack of common nucleophiles such as alcohols or amines.
Synthesis
To a suspension of sodium perborate tetrahydrate (135.374 g., 886.4 mmol) in 500 mL of acetic acid at 55??C was added dropwise 2-bromo-6-fluoroaniline (33.685 g., 177.271 mmol) in 70 mL solution in acetic acid. The reaction mixture was stirred at 55?? C. for an additional 3 h. and then cooled in an ice bath to 0?? C. Insoluble material was removed by filtration through a diatomaceous earth plug and washed with 100 mL of acetic acid. The combined acetic acid was added to 3 liters of ice water with stirring to give a waxy solid which was removed by filtration. The crude solid was dissolved in 250 mL of ethyl acetate and washed three times with 200 mL of 10% aqueous hydrogen chloride, 200 mL of saturated sodium bicarbonate, and 100 mL of brine. Concentrate the solution in vacuum to give 2-bromo-6-fluoronitrobenzene as a red oil in 11.51 g yield.
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