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The Hydroamination of Unactivated Alkenes with Sulfonamides Catalyzed by Phosphomolybdic Acid/SiO

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Phosphomolybdic acid (PMA) supported on silica gel (SiO2) is found to catalyze efficiently the hydroamination of unactivated alkenes with sulfonamides to produce tosyl and mesyl protected secondary amines in excellent yields in short reaction times. The use of reusable solid acid catalyst, phosphomolybdic acid/SiO2 makes this method quite simple, more convenient, cost-effective and environmentally friendly.





Keywords: Heteropoly acids; hydroamination; reusability; secondary amines; sulfonamides; unactivated alkenes

Document Type: Research Article

Publication date: 01 December 2008

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  • Letters in Organic Chemistry publishes original letters on all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is placed on publishing quality papers very rapidly. Letters are processed rapidly and take full advantage of the Internet technology both for the submission and the review of the manuscripts.
    The journal is essential reading for all organic chemists both in academia and industry.
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