Multi-component reaction synthesis of 3-(triphenyl phosphoranylidene) propanoate derivatives via triphenylphosphine and propylate using magnetic CuFe2O4@MIL-101(fe) nanoparticles at room temperature

被引:0
作者
Taheri, Milad [1 ]
Meymandi, Bahare Ghasemi [2 ]
Mehdipourrad, Maysam [3 ]
Alnoaemi, Budor M. [4 ]
Jawhar, Zanko Hassan [1 ]
机构
[1] Lebanese French Univ, Dept Med Lab Sci, Erbil, Kurdistan Regio, Iraq
[2] Islamic Azad Univ, Dept Chem, Yazd Branch, Yazd, Iran
[3] Islamic Azad Univ, Dept Chem Engn, Abadan Branch, Abadan, Iran
[4] Cihan Univ Erbil, Pharm Coll, Erbil, Iraq
关键词
Multi-component reaction (MCRs); triphenylphosphine; room temperature; CuFe2O4@MIL-101(Fe); nanoparticle; SILVER(I)-N-HETEROCYCLIC CARBENE COMPLEXES; BIS-BENZIMIDAZOLIUM SALTS; N-HETEROCYCLIC CARBENES; SILVER(I) COMPLEXES; CRYSTAL-STRUCTURE; ANTIBACTERIAL; ANTICANCER;
D O I
10.1080/00958972.2024.2353299
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A simple, one-pot synthesis of 3-(triphenyl phosphoranylidene) propanoate derivatives has been achieved in moderate to good yields via a multi-component reaction of triphenylphosphine and propylate using CuFe2O4@MIL-101(Fe) nanoparticle at room temperature conditions. The structure of the prepared nanocomposite was confirmed by energy dispersive X-ray spectroscopy (EDX), scanning electron microscopic analysis (SEM), X-ray diffraction (XRD), thermal gravimetry (TGA), and pore size distribution. The catalyst can be recovered magnetically and reused at least four times without significant loss of activity. Our approach demonstrates facile preparation using simple and readily available precursors, with catalysis occurring with good to high yields. This method has advantages in that the reactions are carried out under normal conditions and at room temperature, and the materials are mixed without purification and activation.
引用
收藏
页码:1132 / 1144
页数:13
相关论文
共 62 条
[1]   The clean synthesis and confirmatory structural characterization of new 2-amino-4,8-dihydropyrano[3,2-b]pyran-3-cyano based on Kojic acid [J].
Aghbash, Khadijeh Ojaghi ;
Pesyan, Nader Noroozi ;
Notash, Behrouz .
MONATSHEFTE FUR CHEMIE, 2018, 149 (11) :2059-2067
[2]  
Anastas PT., 1998, GREEN CHEM THEORY PR
[3]  
Andrade CKZ, 2005, CURR ORG CHEM, V9, P195
[4]   A study of cytotoxicity of novel chlorokojic acid derivatives with their antimicrobial and antiviral activities [J].
Aytemir, Mutlu Dilsiz ;
Ozcelik, Berrin .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2010, 45 (09) :4089-4095
[5]   s-Triazinium-based ionic liquid immobilized on silica-coated Fe3O4 magnetic nanoparticles: an efficient and magnetically separable heterogeneous catalyst for synthesis of 2-amino-4,8-dihydropyrano[3,2-b]pyran-3-carbonitrile derivatives for antioxidant and antifungal evaluation studies [J].
Azarifar, Davood ;
Ebrahimiasl, Hakimeh ;
Karamian, Roya ;
Ahmadi-Khoei, Masoumeh .
JOURNAL OF THE IRANIAN CHEMICAL SOCIETY, 2019, 16 (02) :341-354
[6]   Synthesis, characterization, and application of Cu2O and NiO nanoparticles supported on natural nanozeolite clinoptilolite as a heterogeneous catalyst for the synthesis of pyrano[3,2-b]pyrans and pyrano[3,2-c]pyridones [J].
Baghbanian, Seyed Meysam .
RSC ADVANCES, 2014, 4 (103) :59397-59404
[7]  
Banitaba S.H., 2019, Iran, Chem. Commun., V7, P99
[8]   Ultrasound promoted one-pot synthesis of 2-amino-4,8-dihydropyrano [3,2-b]pyran-3-carbonitrile scaffolds in aqueous media: A complementary 'green chemistry' tool to organic synthesis [J].
Banitaba, Sayed Hossein ;
Safari, Javad ;
Khalili, Shiva Dehghan .
ULTRASONICS SONOCHEMISTRY, 2013, 20 (01) :401-407
[9]   The selective reduction of aldehydes using polyethylene glycol-sodium borohydride derivatives as phase transfer reagents [J].
Blanton, JR .
SYNTHETIC COMMUNICATIONS, 1997, 27 (12) :2093-2102
[10]   Sonochemistry in an organocatalytic domino reaction: an expedient multicomponent access to structurally functionalized dihydropyrano[3,2-b] pyrans, spiro-pyrano[3,2-b]pyrans, and spiro-indenoquinoxaline-pyranopyrans under ambient conditions [J].
Borah, Biplob ;
Bora, Jahnu ;
Ramesh, Pambala ;
Chowhan, L. Raju .
RSC ADVANCES, 2022, 12 (20) :12843-12857