Mesoporous TiO <sub>2</sub> /Celite‐Supported Hydrolysis/Decarboxylation of Benzyl Meldrum's Acid Derivatives: Application to the Synthesis of Hydrocinnamic Acid Derivatives

Abstract This study describes a method for transforming benzyl Meldrum's acid (BMA) derivatives into aryl propionic acid (hydrocinnamic acid) derivatives using TiO 2 P25 or Celite surfaces under mild conditions. This selective decarboxylation and hydrolysis process is particularly effective for enolizable Meldrum's acid derivatives. A key feature of this transformation is its chemooselectivity, particularly with acetylated BMA derivatives, which yield the corresponding aryl propionic acids. The method offers several advantages, including compatibility with a wide range of structurally diverse aryl propionic acids, reliance on inexpensive materials, elimination of bases and neutralizing agents, and a simplified work‐up procedure.

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Journal
ChemistrySelect
Published
2024-12-01
DOI
https://doi.org/10.1002/slct.202404128
Citations
1
Primary Topic
Catalytic Cross-Coupling Reactions
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article
Field-Weighted Citation Impact
0.25
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article

Mesoporous TiO 2 /Celite‐Supported Hydrolysis/Decarboxylation of Benzyl Meldrum's Acid Derivatives: Application to the Synthesis of Hydrocinnamic Acid Derivatives

Muthiah Suresh, Raj Bahadur Singh, Anusueya Kumari, Preet Prakash
1 citations
ChemistrySelect
Catalytic Cross-Coupling Reactions
0.25
article

Mesoporous TiO 2 /Celite‐Supported Hydrolysis/Decarboxylation of Benzyl Meldrum's Acid Derivatives: Application to the Synthesis of Hydrocinnamic Acid Derivatives

Muthiah Suresh, Raj Bahadur Singh, Anusueya Kumari, Preet Prakash
article en
1 citations

Abstract

Abstract This study describes a method for transforming benzyl Meldrum's acid (BMA) derivatives into aryl propionic acid (hydrocinnamic acid) derivatives using TiO 2 P25 or Celite surfaces under mild conditions. This selective decarboxylation and hydrolysis process is particularly effective for enolizable Meldrum's acid derivatives. A key feature of this transformation is its chemooselectivity, particularly with acetylated BMA derivatives, which yield the corresponding aryl propionic acids. The method offers several advantages, including compatibility with a wide range of structurally diverse aryl propionic acids, reliance on inexpensive materials, elimination of bases and neutralizing agents, and a simplified work‐up procedure.

ChemistrySelectVol. 9(46)
Central University of Jharkhand (IN), Tamil Nadu Open University (IN)
Openalex Percentile: Top 46%
Catalytic Cross-Coupling Reactions
0.25
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