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Process for the preparation of asymmetric imidazolium salts

机译:制备不对称咪唑鎓盐的方法

摘要

The present invention relates to a process for preparing an asymmetric imidazolium salt of formula 1A, wherein R1 is an aromatic group and R2 is selected from a secondary cycloaliphatic alkyl group and a heteroalkyl group. , R3 and R4 are independently of each other selected from the group consisting of hydrogen, halide and alkyl groups, and A- is an anion. This process comprises a first step of forming a reaction mixture by contacting 1 equivalent of an aniline and 1 equivalent of a compound having an amino group in the presence of at least 4.5 equivalents of Bronsted acid; Forming a solution containing dicarbonyl, 1 equivalent of formaldehyde, and at least 4.5 equivalents of Bronsted acid of formula 4, and adding the reaction mixture formed in the first step; Including. Stirring at a predetermined temperature for a predetermined time, the intermediate asymmetric imidazolium salt 1A is isolated.
机译:本发明涉及一种制备式1A的不对称咪唑鎓盐的方法,其中R1是芳族基团,R2选自仲脂环族烷基和杂烷基。 ,R 3和R 4彼此独立地选自氢,卤化物和烷基,并且A-是阴离子。该方法包括第一步,在至少4.5当量的布朗斯台德酸存在下,使1当量的苯胺与1当量的具有氨基的化合物接触,形成反应混合物。形成包含二羰基,1当量的甲醛和至少4.5当量的式4的布朗斯台德酸的溶液,并添加在第一步中形成的反应混合物;包含。在预定温度下搅拌预定时间,分离出中间体不对称咪唑鎓盐1A。

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