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作 者:曲广淼[1,2] 程杰成[1,3] 丁伟[2] 于涛[2] 李国桥[3]
机构地区:[1]中国石油大学石油天然气工程学院,北京100220 [2]大庆石油学院化学化工学院,黑龙江大庆163318 [3]大庆油田有限责任公司,黑龙江大庆163100
出 处:《石油学报(石油加工)》2010年第2期208-213,共6页Acta Petrolei Sinica(Petroleum Processing Section)
基 金:国家重点基础研究发展计划"973"项目(2005CB221305)资助
摘 要:以邻二甲苯为原料,经Friedel-Crafts酰基化反应、格氏反应、加氢还原反应等步骤合成出8种十六烷基邻二甲苯磺酸钠的异构体。通过正交实验确定了合成中间体3,4-二甲基苯基十六烷基苯酮的最佳工艺条件,即正十四酰氯滴加温度为25℃,邻二甲苯与正十四酰氯的摩尔比为3∶1,反应温度为60℃。在该条件下,3,4-二甲基苯基十六烷基苯酮的收率可达88.23%~90.63%。采用红外光谱、核磁共振氢谱对中间体的结构进行了表征,采用电喷雾质谱对所合成的8种十六烷基邻二甲苯磺酸钠的异构体结构进行了表征。结果表明,合成中间体及最终产物的分子结构与所设计的分子结构相符。Series isomers of hexadecyl o-xlene sulfonates sodium were synthesized by the Fridel-Crafts reaction, the Grignard reaction and hydrogen addition reduction. The optimal processing conditions of the intermediates hyxadecyl o-xylene ketone were determined by the orthogonal experiments, that was the optimal temperature of acyl chloride dropping was 25℃, the optimal molar ratio of o-xylene to acyl chloride was 3:1, the reaction temperature was 60℃, under which the yields of hexadecyl o-xylene ketone could reach up to 88.23%-90.63%. The molecular structures of the intermediate and final products in synthesis of hexadecyl o-xylene sulfonates sodium were characterized by using FT-IR, 1H NMR and ESI-MS methods. The results showed that the molecular structures of the products were the same as the designation.
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