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5-METHOXY-PYRIDIN-3-OL

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5-METHOXY-PYRIDIN-3-OL Basic information

Product Name:
5-METHOXY-PYRIDIN-3-OL
Synonyms:
  • 3-HYDROXY-5-METHOXYPYRIDINE
  • 5-METHOXY-PYRIDIN-3-OL
  • 3-Pyridinol,5-methoxy-(9CI)
  • 5-Methoxypyridin-3-ol, 5-Hydroxypyridin-3-yl methyl ether
  • 5-Methoxy-pyridin-3-ol
  • 3-Pyridinol, 5-methoxy-
  • 5-METHOXY-PYRIDIN-3-OL ISO 9001:2015 REACH
  • 5-Methoxypyridin-3-ol,95%,PY-7888
CAS:
109345-94-0
MF:
C6H7NO2
MW:
125.13
Product Categories:
  • PYRIDINE
Mol File:
109345-94-0.mol
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5-METHOXY-PYRIDIN-3-OL Chemical Properties

Melting point:
147.5-148.5 °C(Solv: ethanol (64-17-5))
Boiling point:
346.7±22.0 °C(Predicted)
Density 
1.190±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
8.93±0.10(Predicted)
Appearance
White to yellow Solid
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/38
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933399990
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5-METHOXY-PYRIDIN-3-OL Usage And Synthesis

Chemical Properties

Off white powder

Uses

5-Methoxypyridin-3-ol is patented as a reagent to prepare various compounds as nicotinic receptor ligands.

Synthesis

445264-60-8

109345-94-0

The general procedure for the synthesis of 5-methoxy-3-hydroxypyridine from 5-methoxy-3-pyridine pinacol borate was as follows: to a stirred suspension of sodium perborate tetrahydrate (7.86 g, 51.06 mmol) in water was added 3-methoxy-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)pyridine (4 g. 17.02 mmol) solution of THF/H2O (80 mL:80 mL) and the reaction was carried out at room temperature. The resulting reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the reaction mixture was extracted with ethyl acetate (200 mL), followed by washing the organic layer with brine and drying over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to give the crude product. The crude product was purified by column chromatography on silica gel (100-200 mesh) using a hexane solution of 20% ethyl acetate as eluent to give a final product of 1.5 g of 5-methoxypyridin-3-ol. LCMS analysis showed a molecular ion peak of 126 (M+H). Step 3 involved the conversion of 3-methoxy-5-hydroxypyridine to 3-methoxy-5-methoxymethoxypyridine.

References

[1] Patent: WO2014/186035, 2014, A1. Location in patent: Page/Page column 156; 157

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