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<ArticleSet>
<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Iranian Journal of Catalysis</JournalTitle>
<Issn>2345-4865</Issn>
<Volume>15</Volume>
<Issue>2</Issue>
<PubDate PubStatus="epublish">
<Year>2025</Year>
<Month>05</Month>
<Day>03</Day>
</PubDate>
</Journal>
<ArticleTitle>Ionic Liquid-mediated Multi-component Reaction Towards the Synthesis of Dihydropyrimidones: An Environmentally Benign Green Protocol</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage></FirstPage>
<LastPage></LastPage>
<ELocationID EIdType="doi">10.57647/j.ijc.2025.1502.18</ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Rakesh P.</FirstName>
<LastName>Chaudhari</LastName>
<Affiliation>Department of Chemistry, Arts and Science College, Bhalod, Dist. – Jalgaon, Maharashtra, India</Affiliation>
<Identifier Source="ORCID">https://orcid.org/0009-0005-5830-3076</Identifier>
</Author>
<Author>
<FirstName>Ganesh R.</FirstName>
<LastName>Chaudhari</LastName>
<Affiliation>Department of Chemistry, Arts and Science College, Bhalod, Dist. – Jalgaon, Maharashtra, India</Affiliation>
<Identifier Source="ORCID">https://orcid.org/0000-0002-9020-0828</Identifier>
</Author>
<Author>
<FirstName>Hemant A.</FirstName>
<LastName>Mahajan</LastName>
<Affiliation>Department of Chemistry, Smt. G. G. Khadse College, Muktainagar, Dist. – Jalgaon, Maharashtra, India</Affiliation>
<Identifier Source="ORCID">https://orcid.org/0009-0003-9513-5396</Identifier>
</Author>
<Author>
<FirstName>Harish R.</FirstName>
<LastName>Talele</LastName>
<Affiliation>Department of Chemistry, TVES’s Dhanaji Nana Mahavidyalaya, Faizpur, Dist. – Jalgaon, Maharashtra, India</Affiliation>
<Identifier Source="ORCID">https://orcid.org/0000-0002-0512-4067</Identifier>
</Author>
</AuthorList>
<PublicationType>Journal Article</PublicationType>
<History>
<PubDate PubStatus="received">
<Year>2025</Year>
<Month>05</Month>
<Day>03</Day>
</PubDate>
</History>
<Abstract>Multi-component reaction (MCR) has notable benefits when compared to traditional linear-type synthetic methods, owing to its adaptable, convergent, and atom-efficient properties. Herein, this study reported the three-component reaction using ethylacetoacetate, aldehydes, and urea in one-step synthesis that provided the 3,4-dihydropyrimidin-2(1H)-ones in excellent yields, such as 5-(Ethoxycarbonyl)-4-(4-chlorophenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one obtained up to 94% of yield. &amp;nbsp;The conversion was led by a catalytic amount of sulfuric acid and ionic liquids as a recyclable green solvent at 80 °C. The recyclable activity of the catalytic system up to three cycles shows excellent yields, ranging from 88% to 94%.
Research Highlights: 

The manuscript reports synthesis of the dihydropyrimidone derivatives by a catalytic system conc. H2SO4 in Ionic Liquids.
Introduce the environment friendly protocol for the synthesis of dihydropyrimidones derivatives. &amp;nbsp;
The presented method following the advantages: short reaction time, mild reaction conditions, and high yields.
The synthesized compounds were characterized by FT-IR, 1H/13C NMR, and Mass analysis.
</Abstract>
<ObjectList>
<Object Type="keyword">
<Param Name="value">Ionic Liquid (ILs)</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Imidazolinium ionic liquids</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Pyridinium ionic liquids</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Dihydropyrimidinones</Param>
</Object>
</ObjectList>
</Article>
</ArticleSet>