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1-(6-METHYL-PYRIDIN-2-YL)-ETHANONE

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1-(6-METHYL-PYRIDIN-2-YL)-ETHANONE Basic information

Product Name:
1-(6-METHYL-PYRIDIN-2-YL)-ETHANONE
Synonyms:
  • 1-(6-METHYL-PYRIDIN-2-YL)-ETHANONE
  • 2-ACETYL-6-METHYLPYRIDINE
  • 1-(6-Methyl-2-pyridinyl)ethanone
  • 6-Acetyl-2-methylpyridine
  • 1-(6-Methylpyridin-2-yl)ethan-1-one
  • 2-ACETYL-6-METHYLPYRIDINE 1-(6-METHYL-PYRIDIN-2-YL)-ETHANONE
  • Ethanone, 1-(6-methyl-2-pyridinyl)-
  • 6-methyl-2-acetylpyridine
CAS:
6940-57-4
MF:
C8H9NO
MW:
135.16
Product Categories:
  • Pyridines
  • Pyridine series
  • Building Blocks
  • Pyridine
Mol File:
6940-57-4.mol
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1-(6-METHYL-PYRIDIN-2-YL)-ETHANONE Chemical Properties

Boiling point:
209℃
Density 
1.036±0.06 g/cm3(Predicted)
Flash point:
84°(183°F)
refractive index 
1.5150
storage temp. 
Inert atmosphere,Room Temperature
pka
3.24±0.10(Predicted)
form 
Solid
color 
Pale yellow
CAS DataBase Reference
6940-57-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-22
Safety Statements 
26-36
HS Code 
2933399990
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1-(6-METHYL-PYRIDIN-2-YL)-ETHANONE Usage And Synthesis

Uses

2-Acetyl-6-methylpyridine is a flavor constituent of rum. A useful synthetic and industrial reagent.

Definition

ChEBI: 2-Acetyl-6-methylpyridine is an aromatic ketone.

Synthesis

71777-66-7

6940-57-4

The general procedure for the synthesis of 2-acetyl-6-methylpyridine from 1-(6-methylpyridin-2-yl)ethan-1-ol is as follows: to a solution of oxalyl chloride (20 mL, 225 mmol, 1.1 eq.) in dichloromethane (300 mL) was slowly added a solution of dimethyl sulfoxide (32 mL, 2.2 eq.) in dichloromethane (400 mL) at -75 °C for 1 hour. The resulting solution was stirred at -75 °C for 10 minutes, then a dichloromethane (600 mL) solution of 1-(6-methylpyridin-2-yl)ethan-1-ol (28 g, 204 mmol, 1 equiv) was slowly added. The reaction mixture was continued to be stirred at the same temperature for 10 minutes, followed by the slow addition of triethylamine (140 mL, 1.02 mol, 5 eq.). The reaction mixture was gradually warmed to 20 °C and stirred for 2 h, after which the reaction was quenched with water (500 mL). The organic phase was separated, dried over magnesium sulfate and concentrated in vacuum to give the crude product. Purification by silica gel column chromatography (eluent ratio 3:1 hexane/ethyl acetate) afforded 2-acetyl-6-methylpyridine (25.36 g, 92% yield).

References

[1] Patent: WO2004/26863, 2004, A1. Location in patent: Page 54

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