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5-(4-(3-二甲氧基甲基硅烷基丙氧基)苯基)-1H-四氮唑的合成 被引量:1

SYNTHESIS OF 5-(4-(3-(DIMETHOXY(METHYL)SILYL) PROPOXY)PHENYL)-1H-TETRAZOLE
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摘要 以对羟基苯甲腈和叠氮钠为主要原料,采用点击化学法环加成合成一种质子导体5-(4-(3-二甲氧基甲基硅烷基丙氧基)苯基)-1H-四氮唑。通过单因素法考察了反应物配比、时间、温度对中间物5-(4-羟基苯基)-四氮唑收率的影响。最佳工艺条件为:n(对羟基苯甲腈):n(叠氮钠)=1:1.4,130℃,24h,50℃下酸化1.5h,中间产物收率达88%;中间产物在75℃下缩合获得目的产物5-(4-(3-二甲氧基甲基硅烷基丙氧基)苯基)-1H-四氮唑,收率可达78%。 Because of conjugate structure, azole nitrogen molecules can form a series of compounds, which have electrochemical stability. 5- ( 4- ( 3- ( Dimethoxy (methyl) silyl ) propoxy) phenyl )-lH-tet- razole(B) was synthesized by click chemistry through cycloaddition and condensation reactions, that could be used for the preparation of new proton exchange membrane. In the synthesis of 5-(4 hydroxyphenol)-1H- tetrazole(A) experiments, the influences of same factors on product yield were investigated, such as the ratio of reactants, reaction time, acidification time, acidification tempera- ture. The opti 1 : 1.4, 130~C tained. In the reaction conditions were , reaction time 24 h, acidified synthesis of 5-(4-(3-(dimeth found as follows: n(4-carbonitrile) : n(sodium azide)= at 50 ℃for about 1.5 h, with the yield of 88% being at- oxy (methyl) silyl) propoxy) phenyl)-1H-tetrazole experi- ments, the yield was 78%. The synthesis process is simple, conditions are mild, with water as sol vent.
出处 《精细石油化工》 CAS CSCD 北大核心 2011年第3期9-12,共4页 Speciality Petrochemicals
基金 河南省轨迹合作项目(编号:104300510009)
关键词 5-(4-羟基苯基)-四氮唑 5-(4-(3-二甲氧基甲基硅烷基丙氧基)苯基)-1H-四氮唑 点击化学 对羟基苯甲腈 叠氮钠 5- (4-hydroxyphenol)-lH-tetrazole 5-( 4-( 3-( dimethoxy (methyl) silyl) propoxy) phenyl )-1H -tetrazole click chemistry 4-hydroxybenzonitrile sodium azide
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参考文献8

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