Beilstein J. Org. Chem.2009,5, No. 24, doi:10.3762/bjoc.5.24
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Herein, we describe the application of titanium dioxide in conjunction with 2,2,6,6-tetramethylpiperidine-1-oxyl radical (TEMPO) as an oxidant in the synthesis of quinoxalines, via the tandem oxidation process (TOP) (Scheme 1).
Results and Discussion
Titanium dioxide in the anatase phase is a
positive holes to the surface and subsequent hydroxyl radical formation [24]. It is believed that a similar interaction is taking place in our system and in conjunction with TEMPO lead to the formation of keto-aldehydes or diketones, which are trapped in situ to produce the required products.
In an attempt
TEMPO for the selective oxidation of alcohols to aldehydes and ketones. In our studies we have been examining similar systems with a view to incorporating them into tandem type processes.
Conclusion
In summary, we have reported the use of titanium dioxide as a tandem oxidation catalyst, demonstrated by
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Graphical Abstract
Scheme 1:
Titanium dioxide/TEMPO mediated synthesis of quinoxalines.
Beilstein J. Org. Chem.2009,5, No. 17, doi:10.3762/bjoc.5.17
characterization of a simplified packed-bed microreactor using an immobilized TEMPO catalyst shown to oxidize primary and secondary alcohols via the biphasic Anelli-Montanari protocol. Oxidations occurred in high yields with great stability over time. We observed that plugs of aqueous oxidant and organic alcohol
100 trials without showing any loss of catalytic activity.
Keywords: alcohol oxidation; flow chemistry; heterogeneous catalysis; microreactors; TEMPO; Introduction
Microreactors have gained attention because they can help run chemical transformations more efficiently, more selectively, and with a
leaching nor the need for catalyst regeneration [22]. Nitroxyl radicals, such as 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO), immobilized on silicates [23][24][25][26][27][28][29][30][31][32], fluorous supports [33], soluble and insoluble polymers [22][34][35][36], magnetic nanoparticles [37], and ionic
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Graphical Abstract
Scheme 1:
Preparation of azide-modified AO resin 2.