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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Synthesis of nitrile coordinated Lewis acids Al(OC(CF3)2R)3 and their application in catalytic epoxide ring-opening reactions
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Synthesis of nitrile coordinated Lewis acids Al(OC(CF3)2R)3 and their application in catalytic epoxide ring-opening reactions

机译:腈配位路易斯酸Al(OC(CF3)2R)3的合成及其在催化环氧化物开环反应中的应用

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摘要

Four nitrile ligated aluminum-based Lewis acids PhCNAl(OC(CF3)2PhCH3)3, CH3CNAI(OC(CF3)2 PhCH3)3, PhCNAl(OC(CF3)2Ph)3 (3), CH3CNAl(OC(CF3)2Ph)3 were synthesized and characterized by nuclear magnetic resonance and infrared spectroscopy, as well as X-ray crystallography. The ring-opening reactions of epoxides with aromatic/aliphatic amines were efficiently catalyzed by compounds 1-4 as catalysts in a concentration of 1 mol% under solvent-free conditions at room temperature, affording 2-amino alcohols in high yields (up to 99%) within 4h. Compound 1, being the best catalyst, yields 70 % product within 10 min.
机译:四种腈连接的铝基路易斯酸PhCNAl(OC(CF3)2PhCH3)3,CH3CNAI(OC(CF3)2 PhCH3)3,PhCNAl(OC(CF3)2Ph)3(3),CH3CNAl(OC(CF3)2Ph)合成了3种,并通过核磁共振和红外光谱以及X射线晶体学表征。在室温下,在无溶剂条件下,以浓度为1 mol%的化合物1-4作为催化剂,可以有效地催化环氧化物与芳族/脂肪族胺的开环反应,从而高产率地获得2-氨基醇(最多99种) %)在4小时内。化合物1是最好的催化剂,可在10分钟内产生70%的产物。

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