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机构地区:[1]北京化工大学新型高分子材料制备与加工北京市重点实验室,北京100029
出 处:《北京化工大学学报(自然科学版)》2009年第4期60-64,共5页Journal of Beijing University of Chemical Technology(Natural Science Edition)
基 金:北京市优秀人才培养专项经费(20041D503001)
摘 要:以联苯二酚为原料经2步反应合成了8-[4′-丙氧基(1,1-联苯)-氧]-辛酸,并对影响产率的因素进行了探讨;通过红外光谱和核磁共振谱表征了8-[4′-丙氧基(1,1-联苯)-氧]-辛酸的化学结构,并用差示扫描量热法和热台偏光显微镜表征了其热致液晶性质。结果表明,第1步合成4′-丙氧基-4-羟基联苯的适宜条件为:n(联苯二酚)∶n(溴代正丙烷)∶n(碱)=1∶1.2∶1,碘化钾用量为4.5%(以联苯二酚质量为基准),加热回流8h;第2步制得8-[4′-丙氧基(1,1-联苯)-氧]-辛酸的适宜条件为;n(碳酸钾)∶n(8-溴辛酸乙酯)∶n(4′-丙氧基-4-羟基联苯)=2∶1.5∶1,相转移剂四丁基溴化铵用量为10%(以4′-丙氧基-4-羟基联苯质量为基准),加热回流24h,将产物在甲醇中水解制得,产率40%,纯度可达94.9%。8-[4'-propoxy(1, 1-biphenyl)-yloxy]-octanoic acid has been synthesized in two steps from 4, 4'-dihydroxybiphenyl and the factors influencing the yield studied. The optimal reaction conditions were found to be as follows: in the first step, with a molar ratio n (4, 4'-dihydroxybiphenyl): n (1-bromopropane): n (alkali) of 1: 1.2 : 1, and the weight of potassium iodide being 4.5 % of that of 4, 4'-dihydroxybiphenyl, under reflux for 8 hours, 4-propoxy-4'-hydroxybiphenyl was obtained; in the second step, with a molar ratio n (potassium carbonate) : n (8-bromooctanoic acid ethyl ester ) : n (4-propoxy-4'-hydroxy) biphenyl of 2 : 1.5 : 1, and with the dosage of phase transfer agent (tetrabutylammonium bromide) being 10 % of that of 4-propoxy-4'-hydroxybiphenyl, refluxing for 24 hours, followed by hydrolysis in methanol, afforded 8-[4'-propoxy (1, 1-biphenyl)-yloxy]-octanoic acid in a yield of 40 % with a purity of 94.9 %. The chemical structure of 8-[4'-propoxy (1, 1-biphenyl)- yloxy]-octanoic acid was confirmed by FTIR, and 1H and 13C NMR spectroscopy. The phase transition and liquid crystalline behavior of 8-[ 4'-propoxy (1, 1-biphenyl)-yloxy]-octanoic acid were characterized by differential scanning calorimetry (DSC) and polarizing microscopy (POM). The experimental results indicated that 8-[4'- propoxy (1, 1-biphenyl)-yloxy]-octanoic acid is a thermotropic liquid crystal.
关 键 词:8-[4'-丙氧基(1 1-联苯)-氧]-辛酸 联苯二酚 8-溴辛酸乙酯 合成 液晶行为
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