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Direct Oxidative Conversion of Alkyl Halides into Nitriles with Molecular Iodine in Aqueous Ammonia

Hideo Togo, Shinpei Iida

Open publisher page 7 citations

Abstract

The direct oxidative conversion of various benzylic alkyl halides and primary alkyl halides into corresponding nitriles was efficiently and simply carried out using molecular iodine in aqueous ammonia. This novel reaction converts alkyl halides into corresponding nitriles without changing the number of carbon atoms.

About this research paper

What this paper is about

The direct oxidative conversion of various benzylic alkyl halides and primary alkyl halides into corresponding nitriles was efficiently and simply carried out using molecular iodine in aqueous ammonia. This novel reaction converts alkyl halides into corresponding nitriles without changing the number of carbon atoms.

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OpenAlex reports 7 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

The direct oxidative conversion of various benzylic alkyl halides and primary alkyl halides into corresponding nitriles was efficiently and simply carried out using molecular iodine in aqueous ammonia. This novel reaction converts alkyl halides into corresponding nitriles without changing the number of carbon atoms.

Key concepts: Chemistry, Halide, Alkyl, Iodine, Ammonia, Aqueous solution, Organic chemistry, Iodine compounds

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