Polyphosphoric Acid Catalyzed C−H Dinitration of Passivated Aromatic Compounds with Potassium Nitrate under Mild Condition

Abstract Dinitroaromatics are valuable organic compounds. However, the high value of these compounds is accompanied by significant risks and formidable challenges. Herein, we report a safe and highly efficient method for the dinitration of various aromatic compounds, using KNO 3 as nitrating agent, polyphosphoric acid as solvent and catalyst. This approach provides a safer and more efficient alternative to the traditional mixed acid system, making it suitable for a range of substrates, especially highly deactivated arenes.

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Publication Details

Journal
European Journal of Organic Chemistry
Published
2024-10-14
DOI
https://doi.org/10.1002/ejoc.202401022
Citations
5
Primary Topic
Catalytic C–H Functionalization Methods
Type
article
Field-Weighted Citation Impact
1.25
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article

Polyphosphoric Acid Catalyzed C−H Dinitration of Passivated Aromatic Compounds with Potassium Nitrate under Mild Condition

Shiyun Li, Xingquan Chen, Bin Wen, Yixiong Jia et al.
5 citations
European Journal of Organic Chemistry
Catalytic C–H Functionalization Methods
1.25
article

Polyphosphoric Acid Catalyzed C−H Dinitration of Passivated Aromatic Compounds with Potassium Nitrate under Mild Condition

Shiyun Li, Xingquan Chen, Bin Wen, Yixiong Jia, H. Chen, Peiran Nan
article en
5 citations

Abstract

Abstract Dinitroaromatics are valuable organic compounds. However, the high value of these compounds is accompanied by significant risks and formidable challenges. Herein, we report a safe and highly efficient method for the dinitration of various aromatic compounds, using KNO 3 as nitrating agent, polyphosphoric acid as solvent and catalyst. This approach provides a safer and more efficient alternative to the traditional mixed acid system, making it suitable for a range of substrates, especially highly deactivated arenes.

European Journal of Organic ChemistryVol. 28(1)
Fuzhou University (CN)
Openalex Percentile: Top 22%
Catalytic C–H Functionalization Methods
1.25
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