Shital B. Sukale, Dipak S. Aher, Laxmikant D. Chavan, Sachin B. Ingole, Sunil G. Shankarwar
{"title":"氧化铝负载的10-钼-2-钨硅酸(H4SiMo10W2O40/Al2O3):合成2,3-二氢喹唑啉-4(1H)- 1衍生物的极活性固体酸催化剂","authors":"Shital B. Sukale, Dipak S. Aher, Laxmikant D. Chavan, Sachin B. Ingole, Sunil G. Shankarwar","doi":"10.1007/s13738-025-03261-5","DOIUrl":null,"url":null,"abstract":"<div><p>Alumina (Al<sub>2</sub>O<sub>3</sub>)-supported 10-molybdo-2-tungstosilicic green acid catalysts were developed by a novel, cheap, environment-friendly approach and utilized in the synthesis of 2,3-dihydroquinazolin-4(1<i>H</i>)-one derivatives. The structure and morphology of the prepared heteropoly acid catalyst were studied by FT-IR, XRD, BET, FE-SEM, HR-TEM, EDX and TG–DTA techniques. The present catalyst shows maximum conversion efficiency in 2,3-dihydroquinazolin-4(1<i>H</i>)-one’s derivatives synthesis. The activity of H<sub>4</sub>SiMo<sub>10</sub>W<sub>2</sub>O<sub>40</sub>/Al<sub>2</sub>O<sub>3</sub> catalysts was tested for the synthesis of 2,3-dihydroquinazolin-4(1<i>H</i>)-ones by the reaction of 2-aminobenzamide and aromatic aldehydes. However, among different catalysts, 20% H<sub>4</sub>SiMo<sub>10</sub>W<sub>2</sub>O<sub>40</sub>/Al<sub>2</sub>O<sub>3</sub> has shown better catalytic activity. Besides, the catalyst was recyclable and reused several times without loss of its catalytic activity. Highest yields of products, mild reaction conditions, short reaction times, non-toxicity, economically affordable catalyst, easy separation of products are some of the advantages of this protocol.</p><h3>Graphical abstract</h3><p>An economic, sustainable, and straightforward environmentally friendly synthesis of 2,3 dihydroquinazolin-4(1H)-ones derivatives from benzaldehyde (1) and 2-aminobenzamide (2) in presence of catalytic amount of H<sub>4</sub>SiMo<sub>10</sub>W<sub>2</sub>O<sub>40</sub>/Al<sub>2</sub>O<sub>3</sub>. Excellent yields, reusability of catalyst, green metrics and environmentally sustainability are the main advantages of the present method.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":676,"journal":{"name":"Journal of the Iranian Chemical Society","volume":"22 8","pages":"1789 - 1804"},"PeriodicalIF":2.3000,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Alumina-supported 10-molybdo-2-tungstosilicic acid (H4SiMo10W2O40/Al2O3): an extremely active solid acid catalyst for the synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives\",\"authors\":\"Shital B. Sukale, Dipak S. Aher, Laxmikant D. Chavan, Sachin B. Ingole, Sunil G. Shankarwar\",\"doi\":\"10.1007/s13738-025-03261-5\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Alumina (Al<sub>2</sub>O<sub>3</sub>)-supported 10-molybdo-2-tungstosilicic green acid catalysts were developed by a novel, cheap, environment-friendly approach and utilized in the synthesis of 2,3-dihydroquinazolin-4(1<i>H</i>)-one derivatives. The structure and morphology of the prepared heteropoly acid catalyst were studied by FT-IR, XRD, BET, FE-SEM, HR-TEM, EDX and TG–DTA techniques. The present catalyst shows maximum conversion efficiency in 2,3-dihydroquinazolin-4(1<i>H</i>)-one’s derivatives synthesis. The activity of H<sub>4</sub>SiMo<sub>10</sub>W<sub>2</sub>O<sub>40</sub>/Al<sub>2</sub>O<sub>3</sub> catalysts was tested for the synthesis of 2,3-dihydroquinazolin-4(1<i>H</i>)-ones by the reaction of 2-aminobenzamide and aromatic aldehydes. However, among different catalysts, 20% H<sub>4</sub>SiMo<sub>10</sub>W<sub>2</sub>O<sub>40</sub>/Al<sub>2</sub>O<sub>3</sub> has shown better catalytic activity. Besides, the catalyst was recyclable and reused several times without loss of its catalytic activity. Highest yields of products, mild reaction conditions, short reaction times, non-toxicity, economically affordable catalyst, easy separation of products are some of the advantages of this protocol.</p><h3>Graphical abstract</h3><p>An economic, sustainable, and straightforward environmentally friendly synthesis of 2,3 dihydroquinazolin-4(1H)-ones derivatives from benzaldehyde (1) and 2-aminobenzamide (2) in presence of catalytic amount of H<sub>4</sub>SiMo<sub>10</sub>W<sub>2</sub>O<sub>40</sub>/Al<sub>2</sub>O<sub>3</sub>. 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Alumina-supported 10-molybdo-2-tungstosilicic acid (H4SiMo10W2O40/Al2O3): an extremely active solid acid catalyst for the synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives
Alumina (Al2O3)-supported 10-molybdo-2-tungstosilicic green acid catalysts were developed by a novel, cheap, environment-friendly approach and utilized in the synthesis of 2,3-dihydroquinazolin-4(1H)-one derivatives. The structure and morphology of the prepared heteropoly acid catalyst were studied by FT-IR, XRD, BET, FE-SEM, HR-TEM, EDX and TG–DTA techniques. The present catalyst shows maximum conversion efficiency in 2,3-dihydroquinazolin-4(1H)-one’s derivatives synthesis. The activity of H4SiMo10W2O40/Al2O3 catalysts was tested for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones by the reaction of 2-aminobenzamide and aromatic aldehydes. However, among different catalysts, 20% H4SiMo10W2O40/Al2O3 has shown better catalytic activity. Besides, the catalyst was recyclable and reused several times without loss of its catalytic activity. Highest yields of products, mild reaction conditions, short reaction times, non-toxicity, economically affordable catalyst, easy separation of products are some of the advantages of this protocol.
Graphical abstract
An economic, sustainable, and straightforward environmentally friendly synthesis of 2,3 dihydroquinazolin-4(1H)-ones derivatives from benzaldehyde (1) and 2-aminobenzamide (2) in presence of catalytic amount of H4SiMo10W2O40/Al2O3. Excellent yields, reusability of catalyst, green metrics and environmentally sustainability are the main advantages of the present method.
期刊介绍:
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