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METHOD OF SYNTHESIS OF 5-SUBSTITUTED-2-CYANO-FURANS

机译:5-取代-2-氰基-呋喃的合成方法

摘要

FIELD: organic chemistry, chemical technology. SUBSTANCE: invention relates to a method of synthesis of 5-substituted-2-cyanofurans of the general formula: where R is a hydrogen or bromine atom, methyl or nitro-group. Method involves an interaction of furan aldehyde of the formula: where R has the above indicated values with hydrazonic acid in chloroform medium, at heating, in the presence of hydrated magnesium perchlorate of the formula Mg(ClO4)2•2,5H2O as a catalyst taken in the mole ratio of the corresponding furan aldehyde, hydrazonic acid and indicated catalyst = 1:1.1:1, respectively, in the range of boiling point values: on start at hydrazonic acid boiling point and then on chloroform boiling point up to nitrogen evolution ceasing. These compounds are used in synthesis of biologically active substances. EFFECT: improved and simplified method of synthesis, increased yield. 1 tbl, 3 ex
机译:领域:有机化学,化学技术。物质:本发明涉及具有以下通式的5-取代的2-氰呋喃的合成方法:<图像文件=“ 00000003.GIF” he =“ 16” id =“ imag00000003” imgContent =“ undefined” imgFormat =“ GIF “ wi =” 28“ />,其中R是氢或溴原子,甲基或硝基。方法涉及下式的呋喃醛的相互作用:其中R具有在水合式Mg(ClO 4 2 &bull; 2,5H < Sub> 2 O作为催化剂,在沸点范围内,相应的呋喃醛,酰肼酸和所示催化剂的摩尔比分别为1:1.1:1:从酰肼酸沸腾开始沸点,然后在氯仿上沸点,直至氮的释放停止。这些化合物用于生物活性物质的合成。效果:改进和简化的合成方法,提高了收率。 1汤匙,3前

著录项

  • 公开/公告号RU2189978C2

    专利类型

  • 公开/公告日2002-09-27

    原文格式PDF

  • 申请/专利权人 KUBANSKIJ GOSUDARSTVENNYJ UNIVERSITET;

    申请/专利号RU20000101486

  • 发明设计人 PAVLOV P.A.;

    申请日2000-01-18

  • 分类号C07D307/56;C07D307/71;

  • 国家 RU

  • 入库时间 2022-08-22 00:28:07

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