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作 者:童华绒 韩军文[1] 王丹[1] 董吉[1] 李小凡[1] 施吉祥[1] 姜波[1]
机构地区:[1]江苏师范大学化学化工学院,江苏徐州221116
出 处:《江苏师范大学学报(自然科学版)》2015年第1期70-73,共4页Journal of Jiangsu Normal University:Natural Science Edition
基 金:国家自然科学基金资助项目(21232004)
摘 要:在微波辐射下,以乙二醇为溶剂,碳酸铯为碱促进剂,将芳甲脒和醛以物质的量之比2∶1反应,合成了一系列1,3,5-三嗪衍生物.该方法具有反应时间短(22~30min)、操作简单和环境友好等优点.产物经红外光谱、核磁共振氢谱、质谱表征,2-对甲苯基-4,6-二苯基-1,3,5-三嗪的结构经单晶X射线衍射分析予以确证.Using ethane-1,2-diol as solvent and Cs2CO3 as base promoter,a series of 1,3,5-triazine derivatives were synthesized via a three-component reaction of aryl carboximidamide and aldehydes with the the ratio of amount of substance 2∶1under microwave irradiation.This method has the advantages of short reaction times(22~30min),simple operation and environment friendliness.The structures of the products were identified by IR,1 HNMR and HRMS.Furthermore,the compound 2-(4-methylphenyl)-4,6-diphenyl-1,3,5-triazine was confirmed by X-ray diffraction.
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