节点文献

3-芳氧基-1,2-丙二醇的合成研究

Study on the Synthesis of 3-Aryloxy-1,2-Propanediols

【作者】 夏汉贵

【导师】 乐治平;

【作者基本信息】 南昌大学 , 有机化学, 2008, 硕士

【摘要】 由于化石能源日益枯竭以及出于环境的考虑,寻找可替代的能源已经受到人类很大的关注。生物柴油可作为石油燃料的替代品,具有可再生性、易生物降解、无毒、含硫量低等优点,属于环境友好的燃料,可具有潜在降低大气污染,减少温室效应。但由生产成本高,制约了其发展空间。生产生物柴油是将植物油和甲醇或乙醇通过酯交换反应制备,同时副产大量的丙三醇。如将丙三醇制备出高附加值产品,将能降低生物柴油生产成本,突破制约生物柴油发展的瓶颈。3-芳氧基-1,2-丙二醇是一种重要的有机合成和医药中间体,用于合成如起释缓神经作用的5-芳氧甲基-2-唑烷酮等。本文以甘油为原料经二步法和以丙烯醇为原料经双氧水环氧化制备缩水甘油,进而与苯酚反应合成3-芳氧基-1,2-丙二醇。研究了工艺条件对反应的影响,探讨了可能的反应的机理。实验结果表明,碱催化剂对一元氯代甘油成环反应制备缩水甘油有较大的影响;W/MCM-41分子筛催化剂能有效催化H2O2氧化丙烯醇制缩水甘油,反应的最佳工艺条件:W/MCM-41催化剂50mg,AAL 1mL,H2O2 2.7mL,H2O 5mL,323K和10 h,缩水甘油的产率为92%;碘化钠用作缩水甘油与苯酚反应的催化剂,以摩尔比为1:1.2,在环己烷为溶剂,碘化钠催化剂30mg,温度72℃,反应时间为3 h的条件下,3-苯氧基-1,2-丙二醇的产率为76%。不同类型的酚和缩水甘油反应的实验结果显示,以环己烷作溶剂,碘化钠作催化剂,较适合于此类型反应。

【Abstract】 Petroleum resources are increasingly exhausted.The living environment in the world is deteriorating due to a lot of the mobil vehicles emission and the greenhouse gas emission.Biodiesel,which is the clean renewable,non-toxic energy and a typical "Green energy",can be as the alternative energy of petroleum to resolve the energy and environment problems.However,the high production costs restricted the development of biodiesel industry.Biodiesel is synthesized by transesterification of vegetable oils with alcohols.A large amount of glycerol is byproducts from the transesterification reaction.It is necessary to produce products with high added value in order to reduce the costs of biodiesel production and break out the bottlenecks. 3-aryloxy-1,2-propanediol is the important organic synthesis and pharmaceutical intermediate,which can be used in synthesis of 5-(aryloxymethyl)-2-oxazolidinone and so on.In the thesis the synthesis of glycidyl and 3-aryloxy-1,2-propanediol were studied.Glycidyl was synthesized by two methods.One was two-step method using glycerol as material,and another was epoxidation method using allyl alcohol as material.3-aryloxy-1,2-propanediol was synthesized from glycidyl and phenols.We studied the effects of technological conditions on synthesis reaction and discussed the synthesis mechanism of 3-aryloxy-1,2-propanediol.The results of test showed that base catalysts had greatly influences on the synthesis of glycidyl from chlorine glycerine by cyclization reaction.W/MCM-41 can effectively catalyze the oxidation from allyl alcohol and H2O2 to form glycidyl.The optimum conditions to form glycidyl using W/MCM-41 catalyst were as fellow:W/MCM-41 catalyst 50 mg,AAL 1 mL,H2O2 2.7mL,H2O 5mL,reaction temperature 50℃and feeding time10 h, glycidyl yield can reach 92%.The optimum conditions to form 3-aryloxy-1, 2-propanediol using cyclehexane as solvent were as fellow:NaI catalyst 30 mg,the ratio of phenol to glycidyl 1:1.2,reaction temperature 72℃and feeding time3 h, 3-phenoxy-1,2-propanediol yield can reach 76%.The results of test implied that the conversion rate and yield of different kinds of phenols reacting with glycidyl,on the whole,were better with cyclehexane as solvent,NaI as catalyst.

  • 【网络出版投稿人】 南昌大学
  • 【网络出版年期】2010年 04期
节点文献中: 

本文链接的文献网络图示:

本文的引文网络