Immobilized proline-based electro-organocatalyst for the synthesis of bis-?-diketone via Knoevenagel condensation reaction
- Title
- Immobilized proline-based electro-organocatalyst for the synthesis of bis-?-diketone via Knoevenagel condensation reaction
- Creator
- Thadathil D.A.; Varghese A.
- Description
- In the quest for more sustainable chemical processes, we devised a technique using electro-organocatalysis to synthesize bis-?-diketone compounds via Knoevenagel condensation of benzaldehyde and dimedone. Our approach involves a modified electrode fabricated via anchoring L-proline onto a carbon fiber paper electrode supported by poly-3,4-diaminobenzoic acid (PDABA), which enhances efficiency in addition to the simple catalyst separation from the reaction mixture in heterogeneous catalysis. The electrochemical and surface topographical studies for the fabricated electrode were carried out, revealing high efficiency in comparison to the bare carbon fiber paper electrode. This electrochemical reaction operates under mild conditions utilizing lithium perchlorate and acetonitrile, yielding high amounts of the desired product. This study showcases a promising pathway for producing valuable organic compounds in an environmentally friendly manner, marking a significant stride forward in sustainable synthesis practices. 2024 Elsevier Ltd
- Source
- Electrochimica Acta, Vol-505
- Date
- 2024-01-01
- Publisher
- Elsevier Ltd
- Subject
- Bis-?-diketone; Electro-organic synthesis; Electro-organocatalyst; Knoevenagel condensation; L-proline
- Coverage
- Thadathil D.A., Department of Chemistry, CHRIST University, Karnataka-, Bengaluru, 560029, India; Varghese A., Department of Chemistry, CHRIST University, Karnataka-, Bengaluru, 560029, India
- Rights
- Restricted Access
- Relation
- ISSN: 134686; CODEN: ELCAA
- Format
- Online
- Language
- English
- Type
- Article
Collection
Citation
Thadathil D.A.; Varghese A., “Immobilized proline-based electro-organocatalyst for the synthesis of bis-?-diketone via Knoevenagel condensation reaction,” CHRIST (Deemed To Be University) Institutional Repository, accessed April 28, 2025, https://archives.christuniversity.in/items/show/12753.