{"title":"NiO@HNTs-SO3H 作为一种新型异相催化剂,用于绿色高效地一步合成 1-(苯并噻唑基氨基)甲基-2-萘酚和四氢苯并[b]吡喃","authors":"Vitisha Vikhe, Akshay Kshirsagar, Bhagwat Uphade, Anil Gadhave","doi":"10.1007/s11164-024-05353-y","DOIUrl":null,"url":null,"abstract":"<div><p>NiO nanoparticles were assembled on the surface of Halloysite nanotubes, which were subsequently further functionalized by sulfonic acid, to create NiO@HNTs-SO<sub>3</sub>H composite. This composite is employed as a heterogeneous catalyst in the one-pot synthesis of 1-(benzothiazolylamino) methyl-2-naphthols starting from aryl aldehyde, β-naphthol and 2-aminobenzothiazole as well as Tetrahydrobenzo[<i>b</i>]pyrans starting from aldehyde, dimedone and malononitrile. The catalyst was examined using Fourier transform infrared (FT-IR), energy dispersive X-ray (EDX), X-ray diffraction (XRD) pattern, and scanning electron microscopy (SEM) images. The synthesized organic compounds were examined using <sup>1</sup>H NMR and <sup>13</sup>C NMR spectroscopy and mass analysis by HRMS. The most notable benefits of the current work are its straightforward setup, gentle reaction conditions, green solvents, excellent yields, ease of purification, high efficiency, and the use of a recoverable and environmentally friendly catalyst. The easy separation and reusability of NiO@HNTs-SO<sub>3</sub>H catalyst after five runs confirmed the stability and effectiveness of the catalyst.</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 9","pages":"4199 - 4227"},"PeriodicalIF":2.8000,"publicationDate":"2024-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"NiO@HNTs-SO3H as a new heterogeneous catalyst for the green and efficient one-pot synthesis of 1-(benzothiazolylamino) methyl-2-naphthols and tetrahydrobenzo[b]pyrans\",\"authors\":\"Vitisha Vikhe, Akshay Kshirsagar, Bhagwat Uphade, Anil Gadhave\",\"doi\":\"10.1007/s11164-024-05353-y\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>NiO nanoparticles were assembled on the surface of Halloysite nanotubes, which were subsequently further functionalized by sulfonic acid, to create NiO@HNTs-SO<sub>3</sub>H composite. This composite is employed as a heterogeneous catalyst in the one-pot synthesis of 1-(benzothiazolylamino) methyl-2-naphthols starting from aryl aldehyde, β-naphthol and 2-aminobenzothiazole as well as Tetrahydrobenzo[<i>b</i>]pyrans starting from aldehyde, dimedone and malononitrile. The catalyst was examined using Fourier transform infrared (FT-IR), energy dispersive X-ray (EDX), X-ray diffraction (XRD) pattern, and scanning electron microscopy (SEM) images. The synthesized organic compounds were examined using <sup>1</sup>H NMR and <sup>13</sup>C NMR spectroscopy and mass analysis by HRMS. The most notable benefits of the current work are its straightforward setup, gentle reaction conditions, green solvents, excellent yields, ease of purification, high efficiency, and the use of a recoverable and environmentally friendly catalyst. The easy separation and reusability of NiO@HNTs-SO<sub>3</sub>H catalyst after five runs confirmed the stability and effectiveness of the catalyst.</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 9\",\"pages\":\"4199 - 4227\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-07-18\",\"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/s11164-024-05353-y\",\"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/s11164-024-05353-y","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
NiO@HNTs-SO3H as a new heterogeneous catalyst for the green and efficient one-pot synthesis of 1-(benzothiazolylamino) methyl-2-naphthols and tetrahydrobenzo[b]pyrans
NiO nanoparticles were assembled on the surface of Halloysite nanotubes, which were subsequently further functionalized by sulfonic acid, to create NiO@HNTs-SO3H composite. This composite is employed as a heterogeneous catalyst in the one-pot synthesis of 1-(benzothiazolylamino) methyl-2-naphthols starting from aryl aldehyde, β-naphthol and 2-aminobenzothiazole as well as Tetrahydrobenzo[b]pyrans starting from aldehyde, dimedone and malononitrile. The catalyst was examined using Fourier transform infrared (FT-IR), energy dispersive X-ray (EDX), X-ray diffraction (XRD) pattern, and scanning electron microscopy (SEM) images. The synthesized organic compounds were examined using 1H NMR and 13C NMR spectroscopy and mass analysis by HRMS. The most notable benefits of the current work are its straightforward setup, gentle reaction conditions, green solvents, excellent yields, ease of purification, high efficiency, and the use of a recoverable and environmentally friendly catalyst. The easy separation and reusability of NiO@HNTs-SO3H catalyst after five runs confirmed the stability and effectiveness of the catalyst.
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.