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New and Efficient Route for the Synthesis of Ketone from Alkyl Halide Using α-Chloro Nitrone as Oxidizing Reagent


Affiliations
1 Organic Chemistry Laboratory, Sikkim Government College, Gangtok, Sikkim 737102, India
     

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Consecutive SN2 reaction of -chloro nitrones are studied with isopropyl halides and the nitrones are found to have remarkable oxidizing properties for the conversion of isopropyl halides to ketones with high yields. In addition, the side product obtained can serve as efficient dipolarophile in 1,3-Dipolar cycloaddition reaction to produce spiro cycloadduct in good yield.


Keywords

α-chloro Nitrone, Ketone Synthesis, Reusable Side Product.
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  • New and Efficient Route for the Synthesis of Ketone from Alkyl Halide Using α-Chloro Nitrone as Oxidizing Reagent

Abstract Views: 185  |  PDF Views: 1

Authors

Bhaskar Chakraborty
Organic Chemistry Laboratory, Sikkim Government College, Gangtok, Sikkim 737102, India
Prawin K. Sharma
Organic Chemistry Laboratory, Sikkim Government College, Gangtok, Sikkim 737102, India

Abstract


Consecutive SN2 reaction of -chloro nitrones are studied with isopropyl halides and the nitrones are found to have remarkable oxidizing properties for the conversion of isopropyl halides to ketones with high yields. In addition, the side product obtained can serve as efficient dipolarophile in 1,3-Dipolar cycloaddition reaction to produce spiro cycloadduct in good yield.


Keywords


α-chloro Nitrone, Ketone Synthesis, Reusable Side Product.