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5-BROMO-3-METHOXY-2-NITROPYRIDINE

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5-BROMO-3-METHOXY-2-NITROPYRIDINE Basic information

Product Name:
5-BROMO-3-METHOXY-2-NITROPYRIDINE
Synonyms:
  • 5-BROMO-3-METHOXY-2-NITROPYRIDINE
  • 3-Bromo-5-methoxy-6-nitropyridine
  • Pyridine, 5-bromo-3-methoxy-2-nitro-
  • 102903
  • 5-BROMO-3-METHOXY-2-NITROPYRIDINE ISO 9001:2015 REACH
CAS:
152684-26-9
MF:
C6H5BrN2O3
MW:
233.02
Product Categories:
  • Pyridine
Mol File:
152684-26-9.mol
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5-BROMO-3-METHOXY-2-NITROPYRIDINE Chemical Properties

Melting point:
112℃
Boiling point:
335℃
Density 
1.730
Flash point:
156℃
storage temp. 
Inert atmosphere,Room Temperature
pka
-8.84±0.10(Predicted)
Appearance
White to off-white Solid
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26
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5-BROMO-3-METHOXY-2-NITROPYRIDINE Usage And Synthesis

Synthesis

50720-12-2

152684-26-9

General procedure for the synthesis of 5-bromo-3-methoxy-2-nitropyridine from 3-bromo-5-methoxypyridine: 3-bromo-5-methoxypyridine (20.91 g, 0.11 mol) was dissolved in concentrated sulphuric acid (63 ml), and nitric acid (5.2 ml, 0.12 mol) was slowly added dropwise in an ice-bath under cooled conditions, and the reaction mixture was stirred for 20 h at room temperature. After completion of the reaction, the mixture was carefully poured into ice water with continuous stirring. The precipitated solid was collected by filtration and washed with cold water. The resulting solid was dissolved in ethyl acetate and the organic layer was washed sequentially with saturated aqueous sodium bicarbonate and saturated brine, followed by drying with anhydrous magnesium sulfate. After filtration to remove the drying agent, the filtrate was concentrated under reduced pressure to afford the target product 5-bromo-3-methoxy-2-nitropyridine (21.97 g, 85% yield) in the form of a light yellow solid. The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz): δ 4.01 (3H, s), 7.68 (1H, d, J = 1.6 Hz), 8.16 (1H, d, J = 1.9 Hz).

References

[1] Patent: US2006/84665, 2006, A1. Location in patent: Page/Page column 70
[2] Patent: WO2010/100127, 2010, A1. Location in patent: Page/Page column 69-70
[3] Acta Chemica Scandinavica, 1993, vol. 47, # 8, p. 805 - 812
[4] Recueil des Travaux Chimiques des Pays-Bas, 1955, vol. 74, p. 1171,1174

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