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METHOD OF PRODUCING 3-ALKYL-2-(2-THIENYL)PYRROLES AND N-VINYL DERIVATIVES THEREOF

机译:生产3-烷基-2-(2-亚硫基)吡咯及其正乙烯基衍生物的方法

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to organic synthesis and specifically to a method of producing 2-(2-thienyl)-3-alkyl pyrroles and N-vinyl derivatives thereof of general formula and , where Alk denotes any linear alkyl substitute. The method is a single-reactor three-component reaction of 2-acylthiophene, hydroxylamine chloride and excess acetylene in the presence of an alkali metal hydroxide with adding sodium bicarbonate to DMSO in an autoclave under acetylene pressure for 1-3 hours at temperature of 80-120°C in a wide range of molar concentration of reactants; molar ratio of reactants acylthiophene: hydroxylamine chloride: acetylene: MOH: DMSO varies in the range of 1:1.0-1.5:2-25:1.5-2.5:30-50.;EFFECT: method of obtaining novel compounds which can be used as monomers for producing electroconductive polymers, particularly as active components of electrodes of polymer rechargeable batteries and electrochromic devices.;2 cl, 4 ex
机译:技术领域本发明涉及有机合成,并且具体地涉及生产通式为和<图像文件=“ 00000014.GIF” he =“ 39” imgContent =“未定义” imgFormat =“ GIF” wi =“ 32 “ />,其中Alk表示任何线性烷基取代基。该方法是在碱金属氢氧化物存在下,将2-酰基噻吩,羟胺氯化物和过量的乙炔进行单反应器三组分反应,然后在高压釜中于80℃的乙炔压力下将碳酸氢钠加入DMSO中1-3小时。 -120°C的反应物摩尔浓度范围很广;反应物酰基噻吩:羟胺氯化物:乙炔:MOH:DMSO的摩尔比在1:1.0-1.5:2-25:1.5-2.5:30-50的范围内变化;效果:获得可以用作新化合物的方法用于生产导电聚合物的单体,特别是用作聚合物可充电电池和电致变色设备的电极的活性成分的单体。; 2 cl,4 ex

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