Synlett 2013; 24(16): 2175-2176
DOI: 10.1055/s-0033-1338973
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© Georg Thieme Verlag Stuttgart · New York

N-Methylmorpholine N-Oxide

Tanya Pieterse
Department of Chemistry, Faculty of Natural and Agricultural Science, University of the Free State, P.O. Box 339, Bloemfontein 9330, South Africa   eMail: pietersetanya@gmail.com
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Publikationsdatum:
26. August 2013 (online)

Introduction

N-Methylmorpholine N-oxide [NMMO (2)] is a light yellow powder with a melting point of 180–184 °C.[1] It is commercially available in both the monohydrate (C5H11NO2·H2O) and anhydrous forms, and is stable under normal conditions.

Apart from being a powerful environmentally friendly solvent for dissolving cellulose,[2] [3] NMMO (2) acts as a strong oxidizing agent and is generally utilized as a stoichiometric oxidant together with TPAP and OsO4 for hydroxy group oxidation[4] and dihydroxylation of olefins.[5] [6]

The oxidative dehydrogenation of amines utilizing gold as the catalyst is also carried out in the presence of NMMO (2), where it acts as a base to afford imines in good yield.[7]

Moreover, NMMO (2) can react as a nucleophile, as is displayed during the reductive work-up of ozonolysis intermediates to afford aldehyde products.[8] [9] One of the advantages of using NMMO versus oxidants like hydrogen peroxide is found in the fact that the byproduct after oxidation [NMM (1)] is very low in basicity.