<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
<PublisherName>OICC Press</PublisherName>
<JournalTitle>Iranian Journal of Catalysis</JournalTitle>
<Issn>2345-4865</Issn>
<Volume>8</Volume>
<Issue>4</Issue>
<PubDate PubStatus="epublish">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</Journal>
<ArticleTitle>Facile synthesis of dihydropyrimidinone derivatives via Biginelli reaction using BrÃ¸nsted acidic ionic liquid [H-NMP]+[CH3SO3]- as an efficient homogeneous catalyst</ArticleTitle>
<VernacularTitle></VernacularTitle>
<FirstPage></FirstPage>
<LastPage></LastPage>
<ELocationID EIdType="doi"></ELocationID>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Hossein</FirstName>
<LastName>Naeimi</LastName>
<Affiliation>Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan, 87317-51167, I.R. Iran.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
<Author>
<FirstName>Zahra Sadat</FirstName>
<LastName>Nazifi</LastName>
<Affiliation>Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan, 87317-51167, I.R. Iran.</Affiliation>
<Identifier Source="ORCID"></Identifier>
</Author>
</AuthorList>
<PublicationType>Journal Article</PublicationType>
<History>
<PubDate PubStatus="received">
<Year>2024</Year>
<Month>02</Month>
<Day>03</Day>
</PubDate>
</History>
<Abstract>In this research, a green, operationally simple, highly efficient and facile cascade Biginelli reaction using various aromatic aldehydes, ethyl acetoacetate, and urea/thiourea has been developed. First, the ionic liquid was prepared from the reaction of 1-methyl-2-pyrolidone with methane sulfonic acid. Then, this ionic liquid was applied as an acidic catalyst in the synthesis of dihydropyrimidinones as a target product under mild conditions. The ionic liquid and resulting products were characterized by physical and spectral data such as melting point, IR, 1HNMR and 13CNMR. The significant advantages of this protocol are short reaction time, excellent yields and easily available starting materials.</Abstract>
<ObjectList>
<Object Type="keyword">
<Param Name="value">Aldehyde</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Catalyst</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Dihydropyrimidinone</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Ionic liquid</Param>
</Object>
<Object Type="keyword">
<Param Name="value">Thiourea</Param>
</Object>
</ObjectList>
</Article>
</ArticleSet>