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Fungicidal dichloro phenyl hydantoin derivs. - prepd. by reacting dichloro phenyl hydantoin with halogenated aldehydes

机译:杀真菌剂二氯苯基乙内酰脲衍生。 -准备使二氯苯基乙内酰脲与卤代醛反应

摘要

New hydantoin derivs. are cpds. of formula (I) (where R is H or CH3; and X and Y are Cl or Br, or X is Cl and Y is CH2Cl). (I) are fungicides with prophylactic and curative activity against phytopathogenic fungi and microorganisms which attack industrial products such as textiles, paints and cellulose-contg. materials. Specific cpds. (I) include 1-(1-hydroxy-2,2,2-trichloroethyl)-3-(3,5-dichlorophenyl)-hydanto- in. In an example, this cpd. is prepd. in 85% yield by stirring chloral with 3-(3,5-dichlorophenyl)-hydantoin in the presence of conc. HCl for 8 hours at 85 degrees C.
机译:新的乙内酰脲衍生。是cpds。式(I)的化合物(其中R为H或CH 3;且X和Y为Cl或Br,或X为Cl且Y为CH 2 Cl)。 (I)是对植物病原性真菌和微生物具有预防和治疗作用的杀真菌剂,这些微生物和微生物会侵害工业产品,例如纺织品,油漆和含纤维素的物质。材料。特定的cpds。 (I)包括1-(1-羟基-2,2,2-三氯乙基)-3-(3,5-二氯苯基)-乙内酰脲。在一个实例中,该cpd。准备好了。在浓溶液存在下,通过将氯醛与3-(3,5-二氯苯基)-乙内酰脲搅拌,以85%的收率。 HCl在85摄氏度下放置8小时。

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