Synthesis of Schiff Base under Solvent-free Condition: As a Green Approach

Abstract This study explores an environmentally friendly approach for synthesizing Schiff bases, a class of compounds with diverse applications. Traditional methods often involve harmful solvents and catalysts, raising concerns about environmental impact. To address these issues, we developed a solvent-free microwave-assisted synthesis of salicylaldimine Schiff bases. This green approach involves directly irradiating salicylaldehyde with various substituted aryl amines, eliminating the need for any additional solvents or catalysts. The successful synthesis of these compounds was confirmed through elemental analysis and thin-layer chromatography (TLC). This solvent-free method offers several advantages, including increased product yield, enhanced purity, and reduced environmental impact. The findings of this study demonstrate a promising alternative for the efficient and sustainable synthesis of Schiff bases.

Institutions

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-12-31
DOI
https://doi.org/10.5281/zenodo.14615440
Primary Topic
Microwave-Assisted Synthesis and Applications
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Synthesis of Schiff Base under Solvent-free Condition: As a Green Approach

Zenodo (CERN European Organization for Nuclear Research)
Microwave-Assisted Synthesis and Applications
article

Synthesis of Schiff Base under Solvent-free Condition: As a Green Approach

article en

Abstract

Abstract This study explores an environmentally friendly approach for synthesizing Schiff bases, a class of compounds with diverse applications. Traditional methods often involve harmful solvents and catalysts, raising concerns about environmental impact. To address these issues, we developed a solvent-free microwave-assisted synthesis of salicylaldimine Schiff bases. This green approach involves directly irradiating salicylaldehyde with various substituted aryl amines, eliminating the need for any additional solvents or catalysts. The successful synthesis of these compounds was confirmed through elemental analysis and thin-layer chromatography (TLC). This solvent-free method offers several advantages, including increased product yield, enhanced purity, and reduced environmental impact. The findings of this study demonstrate a promising alternative for the efficient and sustainable synthesis of Schiff bases.

Zenodo (CERN European Organization for Nuclear Research)
Hanalei Watershed Hui (US)
Responsible consumption and production
Openalex Percentile: Top 59%
Microwave-Assisted Synthesis and Applications
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.