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