Combined process of cyclohexyl cyclohexanecarboxylate synthesis from cyclohexanol and CO catalyzed by the Pd(OAc)2–PPh3–p-toluenesulfonic acid system

N. Sevostyanova, S. Batashev, A. S. Rodionova
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引用次数: 2

Abstract

Objectives. To study the possibility of combining acid-catalytic cyclohexanol dehydration and alkoxycarbonylation of the formed cyclohexene with cyclohexanol and carbon(II) oxide in a single reactor in order to achieve high yields of the target cyclohexyl cyclohexanecarboxylate product under mild conditions using the Pd(OAc)2–PPh3–p-toluenesulfonic acid catalytic system.Methods. The combined process took place in a toluene medium in a periodic steel reactor designed to operate at elevated pressure, equipped with a glass insert, a magnetic stirrer, and a sampler, as well as gas input and discharge devices. The reaction mass with the components of the catalytic system was placed in a glass reactor inside a steel autoclave. The reaction mass samples obtained during the combined process were analyzed by gas–liquid chromatography with a flame ionization detector.Results. The possibility of combining cyclohexanol dehydration catalyzed by p-toluenesulfonic acid monohydrate and formed cyclohexene alkoxycarbonylation with cyclohexanol and CO during catalysis by the Pd(OAc)2–PPh3–p-toluenesulfonic acid system in a single reactor was demonstrated. Under mild conditions (temperature 110°C; CO pressure 2.1 MPa), the target product yield reached 64.8% in 5 h. However, the combined process is complicated by the formation of a cyclohexanecarboxylic acid by-product formed as a result of the cyclohexyl cyclohexanecarboxylate hydrolysis and the cyclohexene hydroxycarbonylation.Conclusions. The reactions of intramolecular acid-catalytic cyclohexanol dehydration and formed cyclohexene alkoxycarbonylation catalyzed by the Pd(OAc)2–PPh3–p-toluenesulfonic acid system can be combined in a single reactor. p-Toluenesulfonic acid can simultaneously act as a catalyst for the cyclohexanol dehydration and a co-catalyst of the palladium–phosphine system of cyclohexene alkoxycarbonylation. The involvement of cyclohexene, representing a product of reversible cyclohexanol dehydration, in the alkoxycarbonylation reaction is a factor in shifting the dehydration reaction equilibrium towards the formation of cyclohexene. Cyclohexanecarboxylic acid is a by-product of the proposed combined process. A factor in the reduction of target product yield is water formed as a result of cyclohexanol dehydration due to the involvement of the latter in the hydrolysis reaction and the course of the cyclohexene hydroxycarbonylation.
Pd(OAc)2 - pph3 -对甲苯磺酸体系催化环己醇与CO合成环己基环己烷羧酸酯的联合工艺
目标。研究酸催化环己醇脱水和生成的环己烯与环己醇和氧化碳(II)在单反应器内烷氧羰基化反应的可能性,以在温和条件下采用Pd(OAc)2 - pph3 -对甲苯磺酸催化体系获得目标环己基环己烷羧酸酯产品的高产率。该组合过程在甲苯介质中进行,在一个设计用于高压操作的周期钢反应器中进行,该反应器配备了玻璃插入件、磁力搅拌器和取样器,以及气体输入和排出装置。反应质量与催化系统的组件被放置在一个玻璃反应器内的钢高压灭菌器。采用气液色谱法和火焰电离检测器对合成过程中得到的反应质量样品进行了分析。证明了Pd(OAc)2 - pph3 -对甲苯磺酸体系在单反应器中催化环己醇脱水和与环己醇和CO形成环己烯烷氧羰基化反应的可能性。在温和条件下(温度110℃;CO压力2.1 MPa), 5 h后目标产物收率达到64.8%。但是,由于环己基环己烷羧酸水解和环己烯羟基羰基化反应生成副产物环己烷羧酸,结合过程较为复杂。分子内酸催化环己醇脱水和Pd(OAc)2 - pph3 -对甲苯磺酸体系催化形成的环己烯烷氧羰基化反应可在单个反应器内同时进行。对甲苯磺酸可以同时作为环己醇脱水的催化剂和环己烯烷氧羰基化钯-膦体系的助催化剂。环己烯是可逆的环己醇脱水产物,其参与烷氧羰基化反应是使脱水反应平衡向生成环己烯转变的一个因素。环己烷羧酸是所提出的组合工艺的副产物。降低目标产物产率的一个因素是由于环己醇在水解反应和环己烯羟基羰基化过程中参与脱水而形成的水。
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