Basic information Safety Supplier Related

1-(1-Methyl-1H-iMidazol-5-yl)ethanone

Basic information Safety Supplier Related

1-(1-Methyl-1H-iMidazol-5-yl)ethanone Basic information

Product Name:
1-(1-Methyl-1H-iMidazol-5-yl)ethanone
Synonyms:
  • 1-(1-Methyl-1H-iMidazol-5-yl)ethanone
  • Ethanone, 1-(1-methyl-1H-imidazol-5-yl)-
  • 1-(3-methylimidazol-4-yl)ethanone
  • 5-Acetyl-1-methylimidazole
CAS:
20970-50-7
MF:
C6H8N2O
MW:
124.14
Mol File:
20970-50-7.mol
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1-(1-Methyl-1H-iMidazol-5-yl)ethanone Chemical Properties

storage temp. 
Sealed in dry,Room Temperature
Appearance
White to yellow Solid
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Safety Information

HS Code 
2933998090
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1-(1-Methyl-1H-iMidazol-5-yl)ethanone Usage And Synthesis

Synthesis

592554-79-5

75-16-1

20970-50-7

General procedure for the synthesis of 1-(1-methyl-1H-imidazol-5-yl)ethanone from the compound (CAS: 592554-79-5) and methylmagnesium bromide: First, the crude product (882) (14.2 mmol) was dissolved in tetrahydrofuran (THF) (100 mL). Methylmagnesium bromide (3 M solution in ether) (22.2 mL) was slowly added under cooling conditions in an ice bath, the titration was controlled to be completed within 10 min and the reaction was carried out under nitrogen (N2) protection. Subsequently, the reaction mixture was warmed up to 40 °C and stirred continuously for 4 h or until the reaction was complete. After completion of the reaction, it was again cooled in an ice bath and the reaction was quenched by slow addition of saturated ammonium chloride (NH4Cl) solution. Initial extraction was carried out with ethyl acetate followed by three extractions with dichloromethane (CH2Cl2). The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and the solvent evaporated. Finally, the product was stored under vacuum to afford crystalline 1-(1-methyl-1H-imidazol-5-yl)ethanone (883) (1.78 g, 74% yield).

References

[1] Patent: US2004/122018, 2004, A1. Location in patent: Page 349

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