首页> 外国专利> 2-Dihalovinyl 3,3-dimethyl cyclopropane carboxylates prodn. - by base catalysed cyclisation of new polyhalo dimethyl hexanoyl halides (NL181176)

2-Dihalovinyl 3,3-dimethyl cyclopropane carboxylates prodn. - by base catalysed cyclisation of new polyhalo dimethyl hexanoyl halides (NL181176)

机译:2-二卤戊基3,3-二甲基环丙烷羧酸酯产品。 -通过新型多卤代二甲基己酰卤的碱催化环化反应(NL181176)

摘要

Process for preparing cyclopropane derivs. of formula (I) comprises treating acid halides (II) with base; (X = Cl or Br; R' = 1-4C alkyl; Y and Z are each Cl or Br; R is CX2=CH- in which case 2 equivs. base are used or CX3CH2- in which case 3 equivs. base are used), =1 equiv. of base in as alkali alkoxide derived from R'OH and the process is carried out in sequential stages with alkoxide treatment as the first or second stage, when it is second stage the base used in the first stage is a tert. amine. (II) are new cpds. (I) (as the free acid) are intermediates for insecticides such as 3-phenoxybenzyl 2-(2,2-dichlorovinyl)3,3-dimethylcyclopropane carbodylate. The process provides (I) without use of the explosive and carcinogenic ethyl diazoacetate required in the known method.
机译:制备环丙烷衍生物的方法。式(I)的化合物包括用碱处理酰卤(II); (X = Cl或Br; R′= 1-4C烷基; Y和Z各自为Cl或Br; R是CX 2 = CH-,在这种情况下使用2当量的碱;或CX3CH 2-,在这种情况下使用3个当量的碱。使用),> = 1当量。以碱的形式作为衍生自R'OH的碱金属醇盐,并且该方法在醇盐处理的第一阶段或第二阶段的连续阶段中进行,当为第二阶段时,第一阶段中使用的碱为叔酸。胺。 (II)是新的cpds。 (I)(作为游离酸)是杀虫剂的中间体,例如3-苯氧基苄基2-(2,2-二氯乙烯基)3,3-二甲基环丙烷甲酸酯。该方法无需使用已知方法所需的爆炸性和致癌性重氮乙酸乙酯即可提供(I)。

著录项

  • 公开/公告号FR2322845A1

    专利类型

  • 公开/公告日1977-04-01

    原文格式PDF

  • 申请/专利权人 ICI LTD;

    申请/专利号FR19770000362

  • 发明设计人

    申请日1977-01-07

  • 分类号C07C53/32;C07C57/02;

  • 国家 FR

  • 入库时间 2022-08-22 23:48:27

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