{"title":"3,5-二氨基-4’-(α-萘基)萘基二苯甲酮的合成与表征 Synthesis and Characterization of (4-([1,1'-Binaphthalen]-4-yl)Phenyl)(3,5-Diaminophenyl)Methanone","authors":"朱雅亮, 段英香, 沈应中","doi":"10.12677/JOCR.2017.51005","DOIUrl":null,"url":null,"abstract":"本文主要讲述了3,5-二氨基-4’-(α-萘基)萘基二苯甲酮的合成。产物及相关的中间体都通过1H NMR, 13C NMR、红外光谱和元素分析进行了表征。该方法简单、产率较高，而且不会对环境造成污染。 This paper mainly described the synthesis of (4-([1,1'-binaphthalen]-4-yl)phenyl)(3,5-diamino- phenyl)methanone. All the compounds and related intermediates were confirmed by 1H NMR, 13C NMR, IR spectrography and element analysis. This method is simple, with a high yield and envi-ronmental-friendly.","PeriodicalId":16596,"journal":{"name":"Journal of Organic Chemistry Research","volume":"27 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2017-03-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.12677/JOCR.2017.51005","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
本文主要讲述了3,5-二氨基-4’-(α-萘基)萘基二苯甲酮的合成。产物及相关的中间体都通过1H NMR, 13C NMR、红外光谱和元素分析进行了表征。该方法简单、产率较高，而且不会对环境造成污染。 This paper mainly described the synthesis of (4-([1,1'-binaphthalen]-4-yl)phenyl)(3,5-diamino- phenyl)methanone. All the compounds and related intermediates were confirmed by 1H NMR, 13C NMR, IR spectrography and element analysis. This method is simple, with a high yield and envi-ronmental-friendly.
3,5-二氨基-4’-(α-萘基)萘基二苯甲酮的合成与表征 Synthesis and Characterization of (4-([1,1'-Binaphthalen]-4-yl)Phenyl)(3,5-Diaminophenyl)Methanone
本文主要讲述了3,5-二氨基-4’-(α-萘基)萘基二苯甲酮的合成。产物及相关的中间体都通过1H NMR, 13C NMR、红外光谱和元素分析进行了表征。该方法简单、产率较高，而且不会对环境造成污染。 This paper mainly described the synthesis of (4-([1,1'-binaphthalen]-4-yl)phenyl)(3,5-diamino- phenyl)methanone. All the compounds and related intermediates were confirmed by 1H NMR, 13C NMR, IR spectrography and element analysis. This method is simple, with a high yield and envi-ronmental-friendly.
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