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Aryl-tetrachloro-aza-propenes and process for the production thereof

机译:芳基四氯氮杂丙烯及其生产方法

摘要

The invention comprises 3-aryl-1,1,3,3-tetrachloro-2-aza -propenes of formula FORM:0981705/C2/1 where Ar represents an aryl radical which may contain substituents such as halogen atoms, aryl radicals, perhalogenated alkyl and cycloalkyl radicals, arylalkyl radicals perhalogenated in the alkyl radical, phenoxy, nitro, nitrile, SO2Cl, ClCO-, RCO-. The compounds may be made by chlorinating an aryl methyl mustard oil ArCH2-N = C = S initially at a temperature below 50 DEG C. to form the arylmethyl isocyanide dichloride, removing the sulphur dichloride formed and further chlorinating at temperatures above 50 DEG C., if desired while exposed to light. The chlorination may be effected with elementary chlorine in an inert solvent or a chlorinating agent such as sulphuryl chloride may be used. Examples describe the preparation of 3 - phenyl - 1,1,3,3 - tetrachlor - 2 - aza - propene-, 3 - (41 - chlorophenyl)-1,1,3,3 - tetrachlor - 2 - aza - propene; 3-(31,41 - dichlorophenyl) - 1,1,3,3 - tetrachlor-2-azapropene.
机译:本发明包含式的3-芳基-1,1,3,3-四氯-2-氮杂-丙烯,其中Ar表示可以包含取代基的芳基,例如卤素原子,芳基,全卤代的烷基和环烷基,在烷基中全卤化的芳基烷基,苯氧基,硝基,腈,SO2Cl,ClCO-,RCO-。可以通过首先在低于50℃的温度下氯化芳基甲基芥子油ArCH2-N = C = S来形成芳基甲基异氰化物二氯化物,除去形成的二氯化硫,并在高于50℃的温度下进一步氯化来制备化合物。 ,如果需要,则使其暴露在光线下。氯化反应可以在惰性溶剂中用元素氯进行,也可以使用氯化剂如磺酰氯。实施例描述了3-苯基-1,1,3,3-四氯-2-氮杂-丙烯-,3-(41-氯苯基)-1,1,3,3-四氯-2-氮杂-丙烯的制备; 3-(31,41-二氯苯基)-1,1,3,3-四氯-2-氮杂丙烯。

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