{"title":"Sawdust-SO3H: A Highly Efficient, Cheap and Recyclable Solid Acid Catalyst for the Synthesis of Quinoline Derivatives under Neat Conditions","authors":"E. Tahanpesar, S. Elhami, M. Mohammadi","doi":"10.12983/IJSRES-2015-P0038-0046","DOIUrl":null,"url":null,"abstract":"Sawdust as a biomass waste material was treated with chlorosulfonic acid and sulfonated sawdust (SD-SO3H) was prepared which characterized with a variation of methods containing TGA, SEM and elemental analysis. This solid acid showed excellent catalytic activity for the synthesis of various quinolines derivatives through the Friedlander condensation of 2-aminoaryl ketones with cyclic and acyclic β-diketone, β- keto esters and cyclic ketone compounds under solvent-free conditions with high yields (70-95%). This new method offers some benefits such as simple procedure, short reaction times, high yields and use of a green, cheap and reusable catalyst.","PeriodicalId":14383,"journal":{"name":"International Journal of Scientific Research in Environmental Sciences","volume":"68 1","pages":"38-46"},"PeriodicalIF":0.0000,"publicationDate":"2015-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Scientific Research in Environmental Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12983/IJSRES-2015-P0038-0046","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Sawdust as a biomass waste material was treated with chlorosulfonic acid and sulfonated sawdust (SD-SO3H) was prepared which characterized with a variation of methods containing TGA, SEM and elemental analysis. This solid acid showed excellent catalytic activity for the synthesis of various quinolines derivatives through the Friedlander condensation of 2-aminoaryl ketones with cyclic and acyclic β-diketone, β- keto esters and cyclic ketone compounds under solvent-free conditions with high yields (70-95%). This new method offers some benefits such as simple procedure, short reaction times, high yields and use of a green, cheap and reusable catalyst.