Non-waste energy and resource-saving heterogeneous catalytic methods of obtaining and transformation of cyclic acetalies and gem-dichlorocyclopropanes

U. G. Borisova, R. Daminev, T. P. Mudrik, G. Z. Raskil’dina
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Abstract

New methods and ways of using heterogeneous zeolite catalysts – H-Y, H-Beta, H-MOR, H-ZSM-5 and micro- meso-porous – H-Ymmm and others in organic synthesis were studied. Using the example of available petrochemical compounds such as polyols, olefins, and dienes, the possibilities of carrying out cyclization and condensation reactions in the presence of zeolites of various structural types are shown. It has been established that the H-Beta zeolite catalyst provides a quantitative yield of ethers and esters during the interaction of olefins – substituted vinyl-gem-dichlorocyclopropanes – with linear alcohols and acids, respectively. It has been determined that the condensation of styrene and an equimolar mixture of 4-hydroxymethyl-1,3-dioxolane and 5-hydroxy-1,3-dioxane in the presence of the H-Beta catalyst proceeds with the formation of ethers, while the ratio of 5 and 6-membered isomeric products = 1.2:1. Multicomponent condensations successfully proceed in one stage in the presence of wide-pore zeolites.
无浪费能源和资源节约型多相催化合成环乙醛和宝石-二氯环丙烷的方法
研究了采用H-Y、H-Beta、H-MOR、H-ZSM-5和微介孔- H-Ymmm等多相沸石催化剂进行有机合成的新方法和新途径。以现有的石化化合物如多元醇、烯烃和二烯烃为例,说明了在不同结构类型的沸石存在下进行环化和缩合反应的可能性。在烯烃-取代的乙烯基宝石-二氯环丙烷-与线性醇和酸的相互作用中,h - β沸石催化剂分别提供了醚和酯的定量产率。经测定,在h - β催化剂的作用下,苯乙烯与4-羟基甲基-1,3-二恶烷和5-羟基-1,3-二恶烷的等摩尔混合物发生缩合反应,生成醚,而5元和6元异构体产物的比例为1.2:1。在宽孔沸石存在的情况下,多组分冷凝在一个阶段成功进行。
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