Li Yun-Fei, Zhang Duo, Wang Hui-Juan, Li Fa-Bao, Sun Liang, Liu Li, Liu Chao-Yang, Asiri Abdullah M, Alamry Khalid A
Hubei Collaborative Innovation Center for Advanced Organic Chemical Materials, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Key Laboratory of Green Preparation and Application for Functional Materials, Ministry of Education, and School of Chemistry and Chemical Engineering , Hubei University , Wuhan 430062 , People's Republic of China.
State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Center for Magnetic Resonance, Wuhan Institute of Physics and Mathematics , Chinese Academy of Sciences , Wuhan 430071 , People's Republic of China.
J Org Chem. 2019 Mar 1;84(5):2922-2932. doi: 10.1021/acs.joc.9b00083. Epub 2019 Feb 15.
A series of scarce N-alkyl-2,5-unsubstituted/monosubstituted fulleropyrrolidines were synthesized in moderate to excellent yields by the simple one-step thermal reaction of [60]fullerene with primary/secondary amines in the presence of paraformaldehyde without the addition of valuable metal salts. Intriguingly, the reaction with primary amines unexpectedly afforded N-alkyl-2,5-unsubstituted fulleropyrrolidines instead of the anticipated 2,5-monosubstituted fulleropyrrolidines. A plausible reaction pathway is proposed to elucidate the above-mentioned reaction process based on the experimental results.
通过[60]富勒烯与伯胺/仲胺在多聚甲醛存在下进行简单的一步热反应,在不添加贵重金属盐的情况下,以中等至优异的产率合成了一系列稀有的N-烷基-2,5-未取代/单取代的富勒吡咯烷。有趣的是,与伯胺的反应意外地得到了N-烷基-2,5-未取代的富勒吡咯烷,而不是预期的2,5-单取代的富勒吡咯烷。基于实验结果,提出了一个合理的反应途径来阐明上述反应过程。