Basic information Safety Supplier Related

3-Bromo-4-chlorofuro[3,2-c]pyridine

Basic information Safety Supplier Related

3-Bromo-4-chlorofuro[3,2-c]pyridine Basic information

Product Name:
3-Bromo-4-chlorofuro[3,2-c]pyridine
Synonyms:
  • 3-Bromo-4-chlorofuro[3,2-c]pyridine
  • Furo[3,2-c]pyridine, 3-bromo-4-chloro-
CAS:
220939-72-0
MF:
C7H3BrClNO
MW:
232.46
Product Categories:
  • Heterocycle-Pyridine series
Mol File:
220939-72-0.mol
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3-Bromo-4-chlorofuro[3,2-c]pyridine Chemical Properties

Boiling point:
305.5±37.0 °C(Predicted)
Density 
1.820±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-1.91±0.40(Predicted)
Appearance
Light yellow to yellow Solid
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3-Bromo-4-chlorofuro[3,2-c]pyridine Usage And Synthesis

Synthesis

31270-80-1

36953-42-1

220939-72-0

Example 543A Synthesis of 3-bromo-4-chlorofuro[3,2-c]pyridine: 4-Chlorofuro[3,2-c]pyridine (commercially available, 10.60 g, 69 mmol) was dissolved in carbon tetrachloride (135 mL) and the solution was cooled to -15°C. Bromine (12.13 g, 80 mmol) was added dropwise to the cooled solution over 15 minutes. After addition, the reaction mixture was stirred at room temperature for 18 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The residue was dissolved in methanol (250 mL), followed by the addition of 20% aqueous sodium hydroxide (35 mL) and continued stirring for 1 hour at room temperature. Methanol was again removed by reduced pressure distillation and the residue was partitioned between water (100 mL) and dichloromethane (50 mL). The organic layers were combined and dried with anhydrous magnesium sulfate. Finally, the solvent was removed by reduced pressure distillation to afford 3-bromo-4-chlorofuro[3,2-c]pyridine 15.45 g (96% yield) as a solid. Mass spectrum (ESI(+)) m/e 232,234 (M + H)+.

References

[1] Patent: US2005/26944, 2005, A1

3-Bromo-4-chlorofuro[3,2-c]pyridineSupplier

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