Synthesis of <i>N</i>‐Substituted Pyrrole‐2,5‐Dicarboxylic Acids from <scp>d</scp>‐Galactaric Acid

Pyrrole-2,5-dicarboxylic acid (PDCA) and its N-substituted derivatives are interesting building blocks for macromolecular applications. However, only a few published procedures describe the synthesis of PDCA derivatives. These procedures often suffer from low yields, the formation of unwanted side products, harsh reaction conditions, the use of toxic and expensive reagents, or the unavailability of certain derivatives. Here, a facile and scalable six-step synthetic route is described, starting from biobased d-galactaric acid, for the production of N-alkylated and N-arylated PDCAs, achieving total yields of up to 45%. In addition, the E-factor of the presented synthesis route is decreased by a factor of 14 compared to already established methods.

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Publication Details

Journal
ChemSusChem
Published
2025-08-18
DOI
https://doi.org/10.1002/cssc.202501106
Citations
1
Primary Topic
Synthesis and Characterization of Pyrroles
Type
article
Field-Weighted Citation Impact
0.94

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article

Synthesis of N‐Substituted Pyrrole‐2,5‐Dicarboxylic Acids from d‐Galactaric Acid

Corinna Urmann, Volker Sieber, Jan‐Simon Jeshua Friedrichs, Kai Stirnweiß
1 citations
ChemSusChem
Synthesis and Characterization of Pyrroles
0.94
article

Synthesis of N‐Substituted Pyrrole‐2,5‐Dicarboxylic Acids from d‐Galactaric Acid

Corinna Urmann, Volker Sieber, Jan‐Simon Jeshua Friedrichs, Kai Stirnweiß
article en
1 citations

Abstract

Pyrrole-2,5-dicarboxylic acid (PDCA) and its N-substituted derivatives are interesting building blocks for macromolecular applications. However, only a few published procedures describe the synthesis of PDCA derivatives. These procedures often suffer from low yields, the formation of unwanted side products, harsh reaction conditions, the use of toxic and expensive reagents, or the unavailability of certain derivatives. Here, a facile and scalable six-step synthetic route is described, starting from biobased d-galactaric acid, for the production of N-alkylated and N-arylated PDCAs, achieving total yields of up to 45%. In addition, the E-factor of the presented synthesis route is decreased by a factor of 14 compared to already established methods.

ChemSusChemVol. 18(19)
The University of Queensland (AU), Weihenstephan-Triesdorf University of Applied Sciences (DE), Stadtwerke Straubing (Germany) (DE), Technical University of Munich (DE)
Bundesministerium für Bildung und Forschung
Clean water and sanitation
Openalex Percentile: Top 23%
Synthesis and Characterization of Pyrroles
0.94
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Synthesis of <i>N</i>‐Substituted Pyrrole‐2,5‐Dicarboxylic Acids from <scp>d</scp>‐Galactaric Acid — Corinna Urmann, Volker Sieber, et al. · ChemSusChem (2025) | TGRS Research Map | TGRS