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3-bromo-2,6-difluorobenzoic acid

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3-bromo-2,6-difluorobenzoic acid Basic information

Product Name:
3-bromo-2,6-difluorobenzoic acid
Synonyms:
  • 3-bromo-2,6-difluorobenzoic acid
  • Benzoic acid, 3-broMo-2,6-difluoro-
  • 3-Bromo-2,6-difluorobenzoic acid 96%
  • 2,6-difluoro-3-bromobenzoic acid
CAS:
28314-81-0
MF:
C7H3BrF2O2
MW:
237
Mol File:
28314-81-0.mol
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3-bromo-2,6-difluorobenzoic acid Chemical Properties

Melting point:
137-139℃
Boiling point:
279℃
Density 
1.872
Flash point:
123℃
storage temp. 
Sealed in dry,Room Temperature
form 
solid
color 
White
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Safety Information

HS Code 
2916310090
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3-bromo-2,6-difluorobenzoic acid Usage And Synthesis

Chemical Properties

Off-white powder

Uses

3-Bromo-2,6-difluorobenzoic Acid is a compound synthesized from an inexpensive starting material 1,3-difluorobenzene.

Synthesis

348-57-2

124-38-9

28314-81-0

(1) Synthesis of 3-bromo-2,6-difluorobenzoic acid: In a dry reaction flask, a hexane solution of 1.6 M n-butyllithium (9.4 mL, 15.0 mmol) was mixed with tetrahydrofuran (20 mL) and cooled to -78 °C. The solution was mixed with tetrahydrofuran (20 mL). To this mixed solution was sequentially added 2,2,6,6-tetramethylpiperidine (2.50 mL, 15.0 mmol) and 1-bromo-2,4-difluorobenzene (2.90 g, 15.0 mmol) and the reaction was stirred for 1 hour at -78 °C. Subsequently, crushed dry ice (5 g) was added to the reaction mixture and stirring was continued at -78 °C for 2 hours. Upon completion of the reaction, the reaction was quenched by the addition of saturated aqueous ammonium chloride solution (5 mL) and the mixture was warmed to room temperature and stirred for 30 minutes. It was diluted by adding water (10 mL) and 1 M hydrochloric acid (30 mL) and extracted with ethyl acetate. The organic phase was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed by concentration under reduced pressure, hexane was added to the residue and the solid product was collected by filtration to afford 3-bromo-2,6-difluorobenzoic acid (2.30 g, 64.6% yield). The product was characterized by 1H-NMR (CDCl3): δ 6.91-6.97 (1H, m), 7.66-7.73 (1H, m).

References

[1] European Journal of Organic Chemistry, 2003, # 23, p. 4618 - 4624
[2] Patent: EP2123644, 2009, A1. Location in patent: Page/Page column 78
[3] Journal of Organic Chemistry, 1990, vol. 55, # 2, p. 773 - 775
[4] Bioorganic and Medicinal Chemistry, 2008, vol. 16, # 23, p. 10001 - 10012

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