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4-METHOXY-PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER

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4-METHOXY-PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER Basic information

Product Name:
4-METHOXY-PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER
Synonyms:
  • 4-METHOXY-PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER
  • METHYL 4-METHOXYPICOLINATE
  • METHYL 4-METHOXYPYRIDINE-2-CARBOXYLATE
  • METHYL 4-METHOXY-2-PYRIDINECARBOXYLATE
  • Methyl 4-methoxypyridine-2-carboxylate 97%
  • 4-METHOXY-2-PYRIDINE CARBOXYLIC ACID METHYL ESTER
  • methyl 4-methoxypyridin-2-carboxyate
  • 4-Methoxy-pyridine-2-carboxylic acid metyl ester
CAS:
29681-43-4
MF:
C8H9NO3
MW:
167.16
EINECS:
685-565-7
Product Categories:
  • Pyridine series
  • Esters
  • blocks
  • Carboxes
  • Pyridines
  • DT
Mol File:
29681-43-4.mol
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4-METHOXY-PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER Chemical Properties

Melting point:
47-50
Boiling point:
280.4±20.0 °C(Predicted)
Density 
1.156±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
DMSO (Slightly), Methanol (Very Slightly)
form 
Solid
pka
2.44±0.10(Predicted)
color 
Pale Yellow
InChI
InChI=1S/C8H9NO3/c1-11-6-3-4-9-7(5-6)8(10)12-2/h3-5H,1-2H3
InChIKey
OJDKENGKKYVJLY-UHFFFAOYSA-N
SMILES
C1(C(OC)=O)=NC=CC(OC)=C1
CAS DataBase Reference
29681-43-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933399990
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4-METHOXY-PYRIDINE-2-CARBOXYLIC ACID METHYL ESTER Usage And Synthesis

Uses

Methyl 4-methoxypicolinate is a useful intermediate for the synthesis of substituted terpyridine ligands for use in protein purification.

Synthesis

98-98-6

67-56-1

124-41-4

29681-43-4

GENERAL STEPS: 2-Pyridinecarboxylic acid (5.0 g, 40.6 mmol) was dissolved in SOCl2 (15 mL) cooled to 0 °C, H2O (950 μL) was added slowly, followed by refluxing the reaction mixture for 1 hour. After the reaction mixture was cooled to room temperature, SOCl2 (15 mL) was added additionally and the reaction was continued to reflux for 2 days. After cooling to room temperature again, a third batch of SOCl2 (15 mL) was added and the mixture was continued to reflux for 2 days. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure and the resulting residue was dissolved in MeOH (30 mL) and refluxed overnight. Subsequently, a solution of NaOMe (4.4 g, 81.2 mmol) in MeOH (50 mL) was added to the reaction system and the reaction was continued at reflux for 2 days. At the end of the reaction, the solvent was removed by distillation under reduced pressure and the residue was dissolved in water and extracted with CHCl3. The organic phases were combined, dried with MgSO4 and concentrated under reduced pressure. The crude product was purified by SiO2 fast column chromatography with the eluent ratio of hexane:AcOEt = 1:1→1:4→1:10 to obtain the target product. Finally, the resulting solid was washed with hexane-Et2O (1:1) to afford methyl 4-methoxypyridine-2-carboxylate (1.8 g, 26% yield) as a light yellow solid.

References

[1] Bulletin of the Chemical Society of Japan, 2015, vol. 88, # 6, p. 784 - 791

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