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首页> 外文期刊>Applied Organometallic Chemistry >Palladium-catalyzed cyanation reaction of aryl halides using K4[Fe(CN)6] as non-toxic source of cyanide under microwave irradiation
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Palladium-catalyzed cyanation reaction of aryl halides using K4[Fe(CN)6] as non-toxic source of cyanide under microwave irradiation

机译:K4 [Fe(CN)6]为无毒氰化物源的钯催化芳基卤化物的氰化反应

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摘要

An efficient method for preparation of aryl nitriles - using [Pd{C6H2(CH2CH2 NH2)-(OMe)2,3,4} (n-Br)]2 complex as an efficient catalyst and K4[Fe(CN)6] as a green cyanide source-from aryl bromides, aryl iodides and aryl chlorides under microwave irradiation has been reported. This complex has been demonstrated to be an active and efficient catalyst for this reaction. Using a catalytic amount of this synthesized palladium complex in DMF at 130 °C led to production of the cyanoarenes in excellent yields in short reaction times.
机译:一种制备芳基腈的有效方法-使用[Pd {C6H2(CH2CH2 NH2)-(OMe)2,3,4}(n-Br)] 2络合物作为有效催化剂,并使用K4 [Fe(CN)6]作为催化剂据报道,在微波辐射下,一种绿色氰化物源来自芳基溴化物,芳基碘化物和芳基氯化物。已经证明该络合物是该反应的活性和有效催化剂。在130°C的DMF中使用催化量的这种合成的钯配合物,可在较短的反应时间内以优异的收率生产氰基芳烃。

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