Oxidation in Flow Using an Ionic Immobilized TEMPO Catalyst on an Ion Exchange Resin

An ionic heterogenized catalyst system for Anelli oxidation has been developed using potassium 4-sulfonato-oxy-2,2,6,6-tetramethylpiperidine-1-yloxyl (TEMPO-4-sulfate) and anion exchange beads as support material. The catalytic oxidation of benzyl alcohol by bis(acetoxy)iodobenzene (BAIB) in acetonitrile with the modified beads gives a 94% yield of benzaldehyde within 60 min (batch operation). The beads give about the same conversion of benzyl alcohol in six consecutive cycles when reused after simple washing, albeit with a somewhat longer half-life time. The TEMPO entity could be removed from the beads using a sodium chloride/sodium hydroxy mixture. Reloading the beads with TEMPO-4-sulfate restored about 80% of their initial catalytic action. This exemplifies that the catalytic activity in a fixed bed can be regained without the need for cleaning and repacking the reactor. Preliminary experiments in a fixed bed show that a constant benzyl alcohol conversion of 84% over 10 residence times (as plug flow) can be achieved by the in-flow execution of the oxidation reaction.

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Publication Details

Journal
Catalysts
Published
2024-08-19
DOI
https://doi.org/10.3390/catal14080542
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.00

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article

Oxidation in Flow Using an Ionic Immobilized TEMPO Catalyst on an Ion Exchange Resin

Gerrit A. Luinstra, J. Gmeiner
Catalysts
Oxidative Organic Chemistry Reactions
article

Oxidation in Flow Using an Ionic Immobilized TEMPO Catalyst on an Ion Exchange Resin

Gerrit A. Luinstra, J. Gmeiner
article en

Abstract

An ionic heterogenized catalyst system for Anelli oxidation has been developed using potassium 4-sulfonato-oxy-2,2,6,6-tetramethylpiperidine-1-yloxyl (TEMPO-4-sulfate) and anion exchange beads as support material. The catalytic oxidation of benzyl alcohol by bis(acetoxy)iodobenzene (BAIB) in acetonitrile with the modified beads gives a 94% yield of benzaldehyde within 60 min (batch operation). The beads give about the same conversion of benzyl alcohol in six consecutive cycles when reused after simple washing, albeit with a somewhat longer half-life time. The TEMPO entity could be removed from the beads using a sodium chloride/sodium hydroxy mixture. Reloading the beads with TEMPO-4-sulfate restored about 80% of their initial catalytic action. This exemplifies that the catalytic activity in a fixed bed can be regained without the need for cleaning and repacking the reactor. Preliminary experiments in a fixed bed show that a constant benzyl alcohol conversion of 84% over 10 residence times (as plug flow) can be achieved by the in-flow execution of the oxidation reaction.

CatalystsVol. 14(8)
Universität Hamburg (DE)
Evonik Stiftung, Evonik Industries
Openalex Percentile: Top 90%
Oxidative Organic Chemistry Reactions
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