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1-(5-METHYL-PYRIDIN-2-YL)-ETHANONE

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1-(5-METHYL-PYRIDIN-2-YL)-ETHANONE Basic information

Product Name:
1-(5-METHYL-PYRIDIN-2-YL)-ETHANONE
Synonyms:
  • 2-ACETYL-5-METHYLPYRIDINE
  • 1-(5-METHYL-PYRIDIN-2-YL)-ETHANONE
  • Ethanone, 1-(5-methyl-2-pyridinyl)-
  • 1-(5-methyl-2-pyridinyl)ethanone(SALTDATA: HCl)
  • 1-(5-Methyl-2-pyridinyl)-Ethanone
  • 1-(5-METHYL-PYRIDIN-2-YL)-ETHANONE ISO 9001:2015 REACH
  • 1-(5-methylpyridin-2-yl)ethan-1-one
CAS:
5308-63-4
MF:
C8H9NO
MW:
135.16
Product Categories:
  • Pyridines
Mol File:
5308-63-4.mol
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1-(5-METHYL-PYRIDIN-2-YL)-ETHANONE Chemical Properties

Boiling point:
105 °C(Press: 13 Torr)
Density 
1.036±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
pka
3.29±0.10(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

HS Code 
2933399990
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1-(5-METHYL-PYRIDIN-2-YL)-ETHANONE Usage And Synthesis

Definition

ChEBI: 2-Acetyl-5-methylpyridine is an aromatic ketone.

Synthesis

3510-66-5

127-19-5

5308-63-4

General procedure for the synthesis of 2-acetyl-5-methylpyridine from 2-bromo-5-methylpyridine and N,N-dimethylacetamide: [Reference Example 35] 5-(5-methyl-2-pyridinyl)-1-(2-pyridinyl)-1H-pyrazole-3-carboxylic acid; [show image] 1) 1-(5-methyl-2-pyridinyl)ethanone; At -78 °C, over 5 min n-butyllithium (1.58 M hexane solution, 24 ml) was added dropwise to a solution of diethyl ether (100 ml) of 2-bromo-5-methylpyridine (5.0 g) and the mixture was stirred for 5 min. Maintaining the same temperature, N,N-dimethylacetamide (3.5 ml) was added to the reaction solution and stirring was continued for 2 hours. After completion of the reaction, water and ethyl acetate were added to the reaction solution and the organic and aqueous phases were separated. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to afford 1-(5-methyl-2-pyridinyl)ethanone (3.43 g, 87% yield) as an oily product.1H-NMR (400 MHz, CDCl3) δ: 2.42 (3H, s), 2.71 (3H, s), 7.62 (1H, dd, J = 1.59, 7.93 Hz), 7.94 (1H, d, J = 7.93 Hz), 8.50 (1H, s).

References

[1] Inorganic Chemistry, 2018,
[2] Patent: EP1698626, 2006, A1. Location in patent: Page/Page column 48
[3] Patent: EP1762568, 2007, A1. Location in patent: Page/Page column 30
[4] Patent: EP1785418, 2007, A1. Location in patent: Page/Page column 38
[5] Chemistry - A European Journal, 2008, vol. 14, # 2, p. 570 - 581

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