呫吨的绿色合成:利用磺化果糖作为高效环保催化剂

A. Kakeshpour, A. Moradi, F. Moradi
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摘要

呫吨具有广泛的生物和治疗特性,包括抗菌、抗病毒和抗炎作用,因此其合成备受关注。氧杂蒽是有机合成中不可或缺的物质,同时也因其作为激光工业染料和检测生物分子的荧光材料所具有的光谱特性而备受重视。尽管已报道了多种合成氧杂蒽的方法,但由于存在效率低、反应时间长、催化剂要求高和使用有害有机溶剂等挑战,因此有必要开发更可持续和更高效的替代品。本研究将磺化果糖作为一种新型绿色催化剂,用于苯甲醛、2-萘酚和二甲酮的缩合反应以合成四氢苯并[a]氧杂蒽-11-酮,以及醛和 2-萘酚的缩合反应以合成 14H-二苯并[a,j]氧杂蒽。果糖的磺化作用可提高其酸度、稳定性和选择性,从而增强其催化活性,因此与纯果糖相比具有显著优势。这些优势包括1.更高的催化活性:磺化果糖酸性的增强缩短了反应时间,提高了产量。2.更高的稳定性:提高催化剂的稳定性可减少降解,延长使用寿命。3.与绿色化学兼容:使用毒性和危害较小的催化剂符合绿色化学原则,可减少环境污染。4.减少对有毒溶剂的需求:使用水和乙醇等环保溶剂,可在较温和的条件下进行反应。5.提高选择性:磺酸基团可提高反应的选择性,从而减少副产物,提高纯度。这种创新方法不仅提高了合成氧杂蒽的效率和可持续性,还证明了使用磺化果糖的经济和环境效益。该方法操作简单、成本低、反应时间短、纯化容易,是对绿色和可持续化学领域的宝贵贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green Synthesis of Xanthenes: Utilizing Sulfonated Fructose as an Efficient and Eco-friendly Catalyst
The synthesis of xanthenes has garnered significant attention due to their extensive biological and therapeutic properties, including antibacterial, antiviral, and anti-inflammatory effects. Xanthenes are indispensable in organic synthesis and are also valued for their spectral properties as dyes in laser industries and fluorescent materials for detecting biological molecules. Despite various methods reported for xanthene synthesis, challenges such as low efficiency, lengthy reaction times, high catalyst requirements, and the use of hazardous organic solvents necessitate the development of more sustainable and efficient alternatives. This study introduces sulfonated fructose as a novel, green catalyst for the condensation reactions of benzaldehyde, 2-naphthol, and dimedone to synthesize tetrahydrobenzo[a]xanthene-11-ones, and aldehyde and 2-naphthol to synthesize 14H-dibenzo[a,j]xanthenes. The sulfonation of fructose enhances its catalytic activity by increasing its acidity, stability, and selectivity, thus providing significant advantages over pure fructose. These include: 1. Higher Catalytic Activity: Enhanced acidity of sulfonated fructose reduces reaction times and increases yields. 2. Greater Stability: Increased stability of the catalyst leads to less degradation and a longer lifespan. 3. Compatibility with Green Chemistry: The use of less toxic and hazardous catalysts aligns with green chemistry principles, reducing environmental pollution. 4. Reduced Need for Toxic Solvents: Reactions can proceed under milder conditions using environmentally friendly solvents like water and ethanol. 5. Improved Selectivity: Sulfonic groups enhance the selectivity of reactions, resulting in fewer by-products and higher purity. This innovative approach not only improves the efficiency and sustainability of xanthene synthesis but also demonstrates the economic and environmental benefits of using sulfonated fructose. The method offers straightforward operation, reduced costs, shorter reaction times, and easier purification, making it a valuable contribution to the field of green and sustainable chemistry.
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