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METHYL 2-PYRIDYLACETATE

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METHYL 2-PYRIDYLACETATE Basic information

Product Name:
METHYL 2-PYRIDYLACETATE
Synonyms:
  • Methyl 2-pyridylacetate,98%
  • NSC 72093
  • methyl 2-(pyridin-2-yl)acetate
  • Pyridin-2-yl-aceticacidMethylester
  • Methyl pyridine-2-acetate
  • Methyl 2-Pyridineacetate 2-Pyridineacetic Acid Methyl Ester 2-Pyridylacetic Acid Methyl Ester
  • 2-PYRIDINEACETIC ACID METHYL ESTER
  • 2-PYRIDYLACETIC ACID METHYL ESTER
CAS:
1658-42-0
MF:
C8H9NO2
MW:
151.16
EINECS:
216-759-8
Product Categories:
  • C7 and C8
  • Heterocyclic Building Blocks
  • Pyridines
  • Heterocyclic Compounds
  • pyridine
  • Building Blocks
  • C8
  • Chemical Synthesis
  • Heterocyclic Building Blocks
Mol File:
1658-42-0.mol
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METHYL 2-PYRIDYLACETATE Chemical Properties

Boiling point:
103 °C/0.5 mmHg (lit.)
Density 
1.119 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.506(lit.)
Flash point:
>230 °F
storage temp. 
Inert atmosphere,Room Temperature
form 
clear liquid
pka
4.35±0.12(Predicted)
color 
Light yellow to Amber to Dark green
InChIKey
ORAKNQSHWMHCEY-UHFFFAOYSA-N
CAS DataBase Reference
1658-42-0
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
HS Code 
29333990

MSDS

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METHYL 2-PYRIDYLACETATE Usage And Synthesis

Chemical Properties

Clear yellow liquid

Synthesis

67-56-1

16179-97-8

1658-42-0

The general procedure for the synthesis of methyl 2-pyridylacetate from methanol and 2-pyridylacetic acid hydrochloride was as follows: the target compound was prepared by referring to literature methods. 2.00 g of 2-pyridine acetic acid hydrochloride (11.5 mmol, 1.00 eq.) was added to a round-bottom flask with 14 mL of methanol. The reaction system was cooled to 0 °C and 2.90 mL of trimethylchlorosilane (23.0 mmol, 2.00 eq.) was slowly added dropwise. After the dropwise addition, the reaction mixture was gradually warmed to room temperature and stirred overnight. After completion of the reaction, the solvent was removed by rotary evaporator under reduced pressure. The residual solid was neutralized by slowly adding 40 mL of saturated aqueous sodium bicarbonate solution to the residual solid. Subsequently, the aqueous phase was extracted with dichloromethane (4 x 40 mL), and the organic phase was combined and dried over anhydrous sodium sulfate. After filtration, the organic phase was concentrated under reduced pressure to afford the crude product methyl 2-pyridylacetate (1.73 g, 11.47 mmol, quantitative yield) as a clear oil. The structure of the product was confirmed by comparing the spectral data of the compound with data reported in the literature.

References

[1] Tetrahedron, 2011, vol. 67, # 24, p. 4435 - 4441
[2] Patent: WO2017/87667, 2017, A1. Location in patent: Paragraph 0069
[3] Journal of the American Chemical Society, 2015, vol. 137, # 32, p. 10246 - 10253
[4] Journal of Organic Chemistry, 2001, vol. 66, # 20, p. 6595 - 6603

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