沉香灰的水提取物:通过多组分反应合成 2-吡啶酮的高效、绿色方法

IF 2.8 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Research on Chemical Intermediates Pub Date : 2024-11-06 DOI:10.1007/s11164-024-05436-w
Aruna N. Patil, Shweta S. Patil, Amit A. Kamble, Suvarta D. Kharade, Dipak S. Gaikwad
{"title":"沉香灰的水提取物:通过多组分反应合成 2-吡啶酮的高效、绿色方法","authors":"Aruna N. Patil,&nbsp;Shweta S. Patil,&nbsp;Amit A. Kamble,&nbsp;Suvarta D. Kharade,&nbsp;Dipak S. Gaikwad","doi":"10.1007/s11164-024-05436-w","DOIUrl":null,"url":null,"abstract":"<div><p>An eco-benign, efficient, cost-effective, high energy-efficient method has been devised for synthesizing diamino-4-phenyl-3,5-dicyano-2-pyridone through a one-pot, three-component reaction. The technique involves the reaction of aryl aldehyde, malononitrile, and cyanoacetic acid hydrazide at 60 °C, utilizing water extract of incense stick ash as a catalyst and recyclable medium. Utilizing water extract as a solvent and catalyst reduces dependency on hazardous and harmful solvents, which are typically non-renewable and contribute to unfavorable emissions. The used incense stick ash was characterized by XRD and EDS analysis. The ash extract consists of metal oxides and carbonates which are basic and can act as catalysts. The reaction proceeds through the Knoevengel reaction, subsequent Michael addition and followed by intramolecular cyclization to furnish <i>N</i>-amino-2-pyridone in good to excellent yields. The structures of the synthesized compounds were confirmed based on IR, <sup>1</sup>H, and <sup>13</sup>C NMR spectral data analysis.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":753,"journal":{"name":"Research on Chemical Intermediates","volume":"50 12","pages":"5901 - 5913"},"PeriodicalIF":2.8000,"publicationDate":"2024-11-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Water extract of incense stick ash: an efficient, greener approach for the synthesis of 2-pyridones via multi-component reaction approach\",\"authors\":\"Aruna N. Patil,&nbsp;Shweta S. Patil,&nbsp;Amit A. Kamble,&nbsp;Suvarta D. Kharade,&nbsp;Dipak S. Gaikwad\",\"doi\":\"10.1007/s11164-024-05436-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>An eco-benign, efficient, cost-effective, high energy-efficient method has been devised for synthesizing diamino-4-phenyl-3,5-dicyano-2-pyridone through a one-pot, three-component reaction. The technique involves the reaction of aryl aldehyde, malononitrile, and cyanoacetic acid hydrazide at 60 °C, utilizing water extract of incense stick ash as a catalyst and recyclable medium. Utilizing water extract as a solvent and catalyst reduces dependency on hazardous and harmful solvents, which are typically non-renewable and contribute to unfavorable emissions. The used incense stick ash was characterized by XRD and EDS analysis. The ash extract consists of metal oxides and carbonates which are basic and can act as catalysts. The reaction proceeds through the Knoevengel reaction, subsequent Michael addition and followed by intramolecular cyclization to furnish <i>N</i>-amino-2-pyridone in good to excellent yields. The structures of the synthesized compounds were confirmed based on IR, <sup>1</sup>H, and <sup>13</sup>C NMR spectral data analysis.</p><h3>Graphical abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":753,\"journal\":{\"name\":\"Research on Chemical Intermediates\",\"volume\":\"50 12\",\"pages\":\"5901 - 5913\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-11-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Research on Chemical Intermediates\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11164-024-05436-w\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research on Chemical Intermediates","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11164-024-05436-w","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

通过单锅三组分反应合成二氨基-4-苯基-3,5-二氰基-2-吡啶酮,设计出了一种生态友好、高效、低成本、高能效的方法。该技术涉及芳基醛、丙二腈和氰乙酸酰肼在 60 ℃ 下的反应,利用沉香灰的水提取物作为催化剂和可回收介质。利用水提取物作为溶剂和催化剂可减少对危险和有害溶剂的依赖,因为这些溶剂通常是不可再生的,而且会造成不利的排放。使用过的香炉灰通过 XRD 和 EDS 分析进行了表征。香灰提取物由金属氧化物和碳酸盐组成,它们具有碱性,可用作催化剂。反应通过 Knoevengel 反应、随后的迈克尔加成和分子内环化反应进行,以良好至极佳的产率合成 N-氨基-2-吡啶酮。根据红外光谱、1H 光谱和 13C NMR 光谱数据分析,确认了合成化合物的结构。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Water extract of incense stick ash: an efficient, greener approach for the synthesis of 2-pyridones via multi-component reaction approach

An eco-benign, efficient, cost-effective, high energy-efficient method has been devised for synthesizing diamino-4-phenyl-3,5-dicyano-2-pyridone through a one-pot, three-component reaction. The technique involves the reaction of aryl aldehyde, malononitrile, and cyanoacetic acid hydrazide at 60 °C, utilizing water extract of incense stick ash as a catalyst and recyclable medium. Utilizing water extract as a solvent and catalyst reduces dependency on hazardous and harmful solvents, which are typically non-renewable and contribute to unfavorable emissions. The used incense stick ash was characterized by XRD and EDS analysis. The ash extract consists of metal oxides and carbonates which are basic and can act as catalysts. The reaction proceeds through the Knoevengel reaction, subsequent Michael addition and followed by intramolecular cyclization to furnish N-amino-2-pyridone in good to excellent yields. The structures of the synthesized compounds were confirmed based on IR, 1H, and 13C NMR spectral data analysis.

Graphical abstract

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
5.70
自引率
18.20%
发文量
229
审稿时长
2.6 months
期刊介绍: Research on Chemical Intermediates publishes current research articles and concise dynamic reviews on the properties, structures and reactivities of intermediate species in all the various domains of chemistry. The journal also contains articles in related disciplines such as spectroscopy, molecular biology and biochemistry, atmospheric and environmental sciences, catalysis, photochemistry and photophysics. In addition, special issues dedicated to specific topics in the field are regularly published.
期刊最新文献
Synthesis of ternary Polyaniline/Bi2S3/NiFe2O4 nanocomposite: as a magnetic separable, reusable, and visible light-responsive photocatalyst for degradation of indigo carmine dye Impact of a homogeneous hydrogen bond catalysis for the ethyl (hetero)arylidene cyanoacetate preparation in the presence of TMDP The effect of modulator in the synthesis of UiO-66(Zr) and UiO-67(Zr) and their performances in catalytic transfer hydrogenation reaction of α-angelica lactone to γ-valerolactone The effect of the introduction of internal acceptor and the variation of π-spacer groups in carbazole-based organic dyes on the photovoltaic performance of dye-sensitized solar cells: a DFT study Green synthesis and DFT study of orthoaminocarbonitrile methyl tetrahydronaphthalene using WEPA: water extract of pomegranate ash as a sustainable catalyst
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1