Synthesis, Characterization, and Optimization of Novel Furan-ring Fused Chalcones via Radical Cyclization of α,β-Unsaturated Ketones and Cyclic Ketone

IF 0.7 4区 化学 Q4 CHEMISTRY, ORGANIC
Emine Vildan Burgaz, Bahareh Noshadi, Mehtap Yakut
{"title":"Synthesis, Characterization, and Optimization of Novel Furan-ring Fused Chalcones via Radical Cyclization of α,β-Unsaturated Ketones and Cyclic Ketone","authors":"Emine Vildan Burgaz, Bahareh Noshadi, Mehtap Yakut","doi":"10.2174/0115701786274099231117113559","DOIUrl":null,"url":null,"abstract":": Novel Furan-ring Fused Chalcones (FFC) were synthesized using a radical cyclization reaction of α,β-unsaturated ketones with cyclic ketone as the model reaction to attain this goal. In this study, traditional and microwave-assisted methods for the efficient and cost-effective synthesis of furan-ring fused chalcones in mild reaction conditions are compared and optimized. The goal is to develop a reliable and adaptable synthetic technique that may be used to produce these useful chalcone derivatives quickly and effectively. The optimal experimental conditions for these reactions were carefully determined using two independent methodologies: conventional (Method A) and microwave (Method B). The results indicated that the proposed method B could be used effectively in the future to synthesize novel furans with short reaction times and acceptable yields (87-94 %), and products were purified by column chromatography and preparative thin layer chromatography (PTLC). All new compounds were characterized by 1H-NMR, 13C-NMR, LC-MS, and elemental analyses. result: The aim of this work was to synthesize a new series of furan-ring fused chalcones using two methods and to show the advantages of microwave when it is compared to conventional synthesis methods. As shown in Table 2, a series of novel compounds (3a-3e) were synthesized in one-step reaction between α,β-unsaturated ketones (1a, 1b), and active methylene compounds (2a-d) (Figure 1). The structures of these compounds were confirmed by several spectroscopic methods (1H NMR, 13C NMR, mass spectra, and elemental analysis). conclusion: We have developed a novel, highly efficient, catalyst-free, green protocol for the one-pot three-component synthesis of furan-ring fused chalcones derivatives. This protocol has the advantages of mild reaction conditions, high yields, convenient operation, and environmental friendliness. The technique has various benefits, most notably a decrease in reaction time, good to high yields, and purer results. This work used microwave irradiation, which reduced the reaction time and produced higher yields than the traditional techniques","PeriodicalId":18116,"journal":{"name":"Letters in Organic Chemistry","volume":"34 4 1","pages":""},"PeriodicalIF":0.7000,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Letters in Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.2174/0115701786274099231117113559","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

: Novel Furan-ring Fused Chalcones (FFC) were synthesized using a radical cyclization reaction of α,β-unsaturated ketones with cyclic ketone as the model reaction to attain this goal. In this study, traditional and microwave-assisted methods for the efficient and cost-effective synthesis of furan-ring fused chalcones in mild reaction conditions are compared and optimized. The goal is to develop a reliable and adaptable synthetic technique that may be used to produce these useful chalcone derivatives quickly and effectively. The optimal experimental conditions for these reactions were carefully determined using two independent methodologies: conventional (Method A) and microwave (Method B). The results indicated that the proposed method B could be used effectively in the future to synthesize novel furans with short reaction times and acceptable yields (87-94 %), and products were purified by column chromatography and preparative thin layer chromatography (PTLC). All new compounds were characterized by 1H-NMR, 13C-NMR, LC-MS, and elemental analyses. result: The aim of this work was to synthesize a new series of furan-ring fused chalcones using two methods and to show the advantages of microwave when it is compared to conventional synthesis methods. As shown in Table 2, a series of novel compounds (3a-3e) were synthesized in one-step reaction between α,β-unsaturated ketones (1a, 1b), and active methylene compounds (2a-d) (Figure 1). The structures of these compounds were confirmed by several spectroscopic methods (1H NMR, 13C NMR, mass spectra, and elemental analysis). conclusion: We have developed a novel, highly efficient, catalyst-free, green protocol for the one-pot three-component synthesis of furan-ring fused chalcones derivatives. This protocol has the advantages of mild reaction conditions, high yields, convenient operation, and environmental friendliness. The technique has various benefits, most notably a decrease in reaction time, good to high yields, and purer results. This work used microwave irradiation, which reduced the reaction time and produced higher yields than the traditional techniques
通过α,β-不饱和酮和环酮的自由基环化合成、表征和优化新型呋喃环融合查耳酮
:为了实现这一目标,本研究以α,β-不饱和酮与环酮的自由基环化反应为模型,合成了新型呋喃环融合查耳酮(FFC)。本研究比较并优化了传统方法和微波辅助方法,以便在温和的反应条件下高效、经济地合成呋喃环融合查耳酮。目的是开发一种可靠且适应性强的合成技术,用于快速有效地生产这些有用的查尔酮衍生物。采用两种独立的方法:传统方法(方法 A)和微波方法(方法 B),仔细确定了这些反应的最佳实验条件。结果表明,建议的方法 B 在未来可有效用于合成新型呋喃,反应时间短,产率可接受(87-94%),产物可通过柱层析和制备薄层色谱法(PTLC)纯化。所有新化合物都通过 1H-NMR、13C-NMR、LC-MS 和元素分析进行了表征:这项工作的目的是用两种方法合成一系列新的呋喃环融合查耳酮,并展示微波合成法与传统合成法相比的优势。如表 2 所示,α,β-不饱和酮(1a, 1b)和活性亚甲基化合物(2a-d)通过一步反应合成了一系列新型化合物(3a-3e)(图 1)。这些化合物的结构通过几种光谱方法(1H NMR、13C NMR、质谱和元素分析)得到了证实:我们开发了一种新型、高效、无催化剂、绿色的一锅三组分合成呋喃环融合查耳酮衍生物的方法。该方案具有反应条件温和、产率高、操作方便和环境友好等优点。该技术具有多种优点,其中最显著的是反应时间缩短、产率从高到低以及结果更纯净。与传统技术相比,这项工作使用微波辐照,缩短了反应时间,产量更高
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Letters in Organic Chemistry
Letters in Organic Chemistry 化学-有机化学
CiteScore
1.30
自引率
12.50%
发文量
135
审稿时长
7 months
期刊介绍: Aims & Scope Letters in Organic Chemistry publishes original letters (short articles), research articles, mini-reviews and thematic issues based on mini-reviews and short articles, in all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is to publish quality papers rapidly by taking full advantage of latest technology for both submission and review of the manuscripts. The journal is an essential reading for all organic chemists belonging to both academia and industry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信