首页> 外文期刊>European Journal of Lipid Science and Technology >Cross-metathesis of methyl 10-undecenoate with diethyl maleate: Formation of an α,ω-diester via a metathesis reaction network
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Cross-metathesis of methyl 10-undecenoate with diethyl maleate: Formation of an α,ω-diester via a metathesis reaction network

机译:10-十一碳烯酸甲酯与马来酸二乙酯的交叉复分解反应:通过复分解反应网络形成α,ω-二酯

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摘要

The cross-metathesis of methyl 10-undecenoate 1 derived from castor oil as a renewable raw material with diethyl maleate 2 was investigated. These reactions were carried out with several phosphine and N-heterocyclic carbene ruthenium catalysts. The reaction conditions were optimised for high conversions in combination with high cross-metathesis selectivity. This single-step and atom-economic synthetic method illustrates an efficient and selective preparation procedure of linearα,ω-dicarboxylic acid esters starting from renewable resources and comparatively inexpensive base chemicals. Further byproducts are hardly obtained due to their consumption in secondary metathesis reactions. Hence, a sustainable alternative for polyamide and polyester monomers is presented.
机译:研究了作为可再生原料的蓖麻油中的10-十一碳烯酸甲酯1与马来酸二乙酯2的复分解反应。这些反应是用几种膦和N-杂环卡宾钌催化剂进行的。优化了反应条件,以实现高转化率和高交叉复分解选择性。这种单步且原子经济的合成方法说明了从可再生资源和相对便宜的基础化学品开始的线性,α-ω-二羧酸酯的有效和选择性制备方法。由于在次级复分解反应中消耗了副产物,因此很难获得其他副产物。因此,提出了聚酰胺和聚酯单体的可持续替代品。

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