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2-Fluoro-4-Bromo-3-Picoline

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2-Fluoro-4-Bromo-3-Picoline Basic information

Product Name:
2-Fluoro-4-Bromo-3-Picoline
Synonyms:
  • 2-Fluoro-4-bromo-3-methylpyridine
  • 2-Fluoro-4-Bromo-3-Picoline
  • 4-Bromo-2-fluoro-3-methylpyridine
  • 4-BROMO-2-FLUORO-3-METHYLPYRIDIN
  • Pyridine, 4-bromo-2-fluoro-3-methyl-
  • 2-Fluoro-4-Bromo-3-Picoline ISO 9001:2015 REACH
  • bromo-4 fluoro-2 methyl-3 pyridine
CAS:
128071-79-4
MF:
C6H5BrFN
MW:
190.01
Product Categories:
  • Pyridine
Mol File:
128071-79-4.mol
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2-Fluoro-4-Bromo-3-Picoline Chemical Properties

Boiling point:
220℃
Density 
1.592
Flash point:
87℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
1.05±0.10(Predicted)
form 
Oil
color 
Colourless
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Safety Information

RIDADR 
UN1993
HS Code 
2933399990
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2-Fluoro-4-Bromo-3-Picoline Usage And Synthesis

Uses

2-Fluoro-4-bromo-3-pyridine is an organic compound that is often used as an intermediate in chemical synthesis, especially in the synthesis of drugs and pesticides.

Synthesis

128071-98-7

74-88-4

128071-79-4

A solution of lithium diisopropylammonium (LDA, 2M, 8.5 mL) was added slowly and dropwise to a solution of 4-bromo-2-fluoropyridine (2 g, 11.3 mmol) in tetrahydrofuran (THF, 40 mL) at -78 °C. The reaction mixture was stirred continuously at -78 °C for 1 h, followed by dropwise addition of iodomethane (4.8 g, 34 mmol). After continued stirring at -78 °C for 1 h, the reaction mixture was allowed to slowly warm up to room temperature over a period of 1 h. The reaction was completed with the addition of iodomethane (4.8 g, 34 mmol). Upon completion of the reaction, the reaction was quenched with saturated sodium bicarbonate (NaHCO3) solution, followed by the addition of an aqueous solution of ammonium chloride (NH4Cl, 50 mL) at 0 °C and extraction with ethyl acetate (EA, 60 mL x 3). The organic layers were combined, washed with brine (60 mL), dried over anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate, PE/EtOAc) to afford 2-fluoro-3-methyl-4-bromopyridine (1 g, 47% yield) as a yellow solid.1H-NMR (400 MHz, CDCl3) δppm: 2.35 (s, 3H), 7.36 (d, 1H), 7.86 (d, 1H).

References

[1] Patent: WO2017/221092, 2017, A1. Location in patent: Paragraph 00188

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