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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Utilisation of 1,3-dialkylimidazolium-2-carboxylates as CO2-carriers in the presence of Na+ and K+: application in the synthesis of carboxylates, monomethylcarbonate anions and halogen-free ionic liquids
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Utilisation of 1,3-dialkylimidazolium-2-carboxylates as CO2-carriers in the presence of Na+ and K+: application in the synthesis of carboxylates, monomethylcarbonate anions and halogen-free ionic liquids

机译:Na +和K +存在下1,3-二烷基咪唑-2-羧酸盐作为CO2载体的用途:在合成羧酸盐,一甲基碳酸根阴离子和无卤离子液体中的应用

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摘要

1,3-Dialkylimidazolium-2-carboxylate compounds have recently been fully characterised. Here we describe the utilisation of 1,3-dimethyl (1a) and 1-butyl-3-methyl-imidazolium-2-carboxylate (1b) in a carboxylation reaction with transfer of the CO2 moiety to benzoylacetone and methanol for the synthesis, in high yield, of benzoylacetate and monoalkylcarbonate anions, respectively. Conversely, when compounds 1a and b are reacted with carbonylic substrates lacking C-H active bonds, a product resulting from nucleophilic attack of the 1,3-dialkylimidazol-2-ylidene species on the carbonyl moiety is obtained. The reported reactions can find applications in organic synthesis and in the synthesis of halogen-free ionic liquids. (C) 2005 Elsevier Ltd. All rights reserved.
机译:最近已完全表征了1,3-二烷基咪唑鎓-2-羧酸酯化合物。在这里,我们描述了在羧化反应中利用1,3-二甲基(1a)和1-丁基-3-甲基咪唑-2-羧酸盐(1b)将CO2部分转移至苯甲酰丙酮和甲醇进行合成的过程,苯甲酰乙酸根和碳酸单烷基酯的高收率。相反,当化合物1a和b与缺乏C-H活性键的羰基底物反应时,获得了由1,3-二烷基咪唑-2-亚烷基在羰基部分上的亲核进攻而得到的产物。报道的反应可用于有机合成和无卤离子液体的合成中。 (C)2005 Elsevier Ltd.保留所有权利。

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