{"title":"Synthesis of 2-hydroxy-5(3-methylcyclohexyl)aceto- and benzophenones in the presence of a nano-catalytic system","authors":"G. Haydarli, Ch. K. Rasulov, N. M. Alieva","doi":"10.32758/2782-3040-2023-0-2-22-26","DOIUrl":null,"url":null,"abstract":"The results of studying of the cycloalkylation reaction of phenol with 3-methylcyclohexene in the presence of zeolite Y impregnated with phosphoric acid are presented. It was found that in order to achieve a high yield (71.2%) and selectivity (93.7%) during the cycloalkylation reaction of phenol with 3-methylcyclohexene, the reaction conditions should be as follows: reaction temperature 120 oC, molar ratio of phenol to 3-methylcyclohexene 1:1, volume velocity 0.5 h-1. The results of the synthesis of 2-hydroxy-5(3-methylcyclohexyl) aceto- and benzophenones by the reaction of p-(3-methylcyclohexyl) phenol with acetic acid (AcOH) and benzoyl chloride (BzCl) with the participation of nanosized ZnCl2 as a catalyst are presented. It was found that at a temperature of 140 oC, a reaction time of 40 minutes, and a molar ratio of p-(3-methylcyclohexyl) phenol to AcOH (BzCl) of 1:2, the yield of the target products was 63.3-66.7%.","PeriodicalId":23763,"journal":{"name":"World of petroleum products","volume":"42 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"World of petroleum products","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.32758/2782-3040-2023-0-2-22-26","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
The results of studying of the cycloalkylation reaction of phenol with 3-methylcyclohexene in the presence of zeolite Y impregnated with phosphoric acid are presented. It was found that in order to achieve a high yield (71.2%) and selectivity (93.7%) during the cycloalkylation reaction of phenol with 3-methylcyclohexene, the reaction conditions should be as follows: reaction temperature 120 oC, molar ratio of phenol to 3-methylcyclohexene 1:1, volume velocity 0.5 h-1. The results of the synthesis of 2-hydroxy-5(3-methylcyclohexyl) aceto- and benzophenones by the reaction of p-(3-methylcyclohexyl) phenol with acetic acid (AcOH) and benzoyl chloride (BzCl) with the participation of nanosized ZnCl2 as a catalyst are presented. It was found that at a temperature of 140 oC, a reaction time of 40 minutes, and a molar ratio of p-(3-methylcyclohexyl) phenol to AcOH (BzCl) of 1:2, the yield of the target products was 63.3-66.7%.