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3-BROMO-2-CHLORO-4-PICOLINE

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3-BROMO-2-CHLORO-4-PICOLINE Basic information

Product Name:
3-BROMO-2-CHLORO-4-PICOLINE
Synonyms:
  • 2-CHLORO-3-BROMO-4-PICOLINE
  • 3-BROMO-2-CHLORO-4-METHYLPYRIDINE
  • 3-BROMO-2CHLORL-4-PICOLINE
  • 2-Chloro-3-bromo-4-methylpyridine
  • 3-Bromo-2-chloro-4-methyl...
  • 3-Bromo-2-chloro-4-methylprinine
  • 3-Bromo-2-chloro-4-methylpyridine 97%
  • 3-BROMO-2-CHLORO-4-PICOLINE
CAS:
55404-31-4
MF:
C6H5BrClN
MW:
206.47
Product Categories:
  • Heterocycle-Pyridine series
Mol File:
55404-31-4.mol
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3-BROMO-2-CHLORO-4-PICOLINE Chemical Properties

Boiling point:
250.3±35.0 °C(Predicted)
Density 
1.624±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
0.17±0.10(Predicted)
form 
solid
color 
Light yellow
CAS DataBase Reference
55404-31-4(CAS DataBase Reference)
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Safety Information

HS Code 
2933399990
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3-BROMO-2-CHLORO-4-PICOLINE Usage And Synthesis

Synthesis

133627-45-9

55404-31-4

(1) Synthesis of 3-bromo-2-chloro-4-methylpyridine 3-Amino-2-chloro-4-methylpyridine (2 g) was dissolved in a solvent mixture of 48% aqueous hydrogen bromide solution (17 mL) and water (12 mL). Sodium nitrite (2.5 g) was added to the solution in batches at 0 °C. Subsequently, bromine (22 mL) was added slowly and dropwise. The reaction mixture was gradually warmed to room temperature and stirred continuously for 12 hours. Upon completion of the reaction, the pH was adjusted to neutral with 5N aqueous sodium hydroxide and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. After filtration to remove the drying agent, the filtrate was concentrated under reduced pressure to afford the target product 3-bromo-2-chloro-4-methylpyridine (1.7 g). The product was characterized by 1H-NMR (400 MHz, CDCl3): δ 2.51 (s, 3H), 7.01-7.24 (m, 1H), 8.06-8.35 (m, 1H).

References

[1] Patent: US2013/143907, 2013, A1. Location in patent: Paragraph 0475; 0476

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