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Synthesis of 2,5-disubstituted pyrroles via dehydrogenative condensation of secondary alcohols and 1,2-amino alcohols by supported platinum catalysts

机译:负载型铂催化剂通过仲醇与1,2-氨基醇的脱氢缩合反应合成2,5-二取代吡咯

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摘要

Direct synthesis of 2,5-disubstituted pyrroles has been achieved via acceptorless dehydrogenative heterocyclization of 1,2-aminoalcohols and secondary alcohols by utilizing a heterogeneous carbon-supported Pt catalyst (Pt/C). The optimized method gave 92% yield of 2-ethyl-5-phenyl-1H-pyrrole as a desired product from 2-amino-1-butanol and 1-phenylethanol in the presence of 0.1 mol% of Pt/C and 1.1 equiv. of KOtBu. It has been revealed that Pt/C demonstrates superior catalytic activity to a number of catalysts tested in this study including other transition metal-loaded carbon and various metal-oxide-supported Pt catalysts. In addition, the turnover number (TON) obtained in the present system was found to be higher than those obtained in previously-reported catalytic systems. It is significant that the Pt/C catalyst could be recycled as a heterogeneous catalyst without significant loss in the activity and showed a wide substrate scope for the 2,5-disubstituted pyrrole forming process.
机译:通过利用多相碳载Pt催化剂(Pt / C)通过1,2-氨基醇和仲醇的无受体脱氢杂环化,已经实现了2,5-二取代吡咯的直接合成。优化的方法在0.1mol%的Pt / C和1.1当量的存在下,由2-氨基-1-丁醇和1-苯基乙醇以92%的收率得到作为所需产物的2-乙基-5-苯基-1H-吡咯。 KOtBu。已经发现,Pt / C具有比本研究中测试的许多催化剂(包括其他过渡金属负载的碳和各种金属氧化物负载的Pt催化剂)优越的催化活性。另外,发现在本系统中获得的周转数(TON)高于在先前报告的催化系统中获得的周转数(TON)。值得注意的是,Pt / C催化剂可作为多相催化剂循环使用,而不会显着降低活性,并显示出2,5-二取代吡咯形成过程中较宽的底物范围。

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