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To probe the substrate scope of the reaction, more aryl iodides and bromides were chosen to react with phenylactylene using 1 mol % catalyst 3a with 2 eq K2CO3 in DMSO (2 mL) in air (Table 3). The results showed that 3a could not only catalyze the cross-coupling reaction of phenylacetylene with more reactive aryl iodides, but also could catalyze the reaction in good to moderate yield (55% -86%) with less reactive aryl bomides in the absence of copper co-catalysis. To an oven-dried 50 mL of r.b.f. containing 2a , PdCl2 , K2CO3 and NaBr with a septum was injected into pyridine (5 mL) under argon. |
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為了探測反應的底物范圍,用更多芳基碘化物和溴化物與苯乙炔反應,反應調(diào)節(jié)為1摩爾%的催化劑3a和2當量的K2CO3在DMSO(2mL)及空氣條件下進行(表3)。結(jié)果表明,3a不僅可以催化苯乙炔與多個反應性芳基碘發(fā)生交叉偶聯(lián)反應,也可以在無銅共催化存在條件下催化苯乙炔與反應性低的芳基溴化物發(fā)生反應,產(chǎn)率中等到良好(55%-86%)。 在帶隔膜干燥烘箱中,向含有2a、PdCl2、K2CO3和溴化鈉的50毫升r.b.f.在氬氣條件下注入吡啶(5毫升)。 |
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