Instituto de Productos Naturales y Agrobiología, Consejo Superior de Investigaciones Científicas, Astrofísico Francisco Sánchez 3, 38206 La Laguna, Spain.
Doctoral and Postgraduate School, Universidad de La Laguna, Apartado Postal 456, 38200 La Laguna, Spain.
Molecules. 2021 Jul 6;26(14):4120. doi: 10.3390/molecules26144120.
A novel organocatalytic multicomponent cyanovinylation of aldehydes was designed for the synthesis of conjugated cyanomethyl vinyl ethers. The reaction was implemented for the synthesis of a 3-substituted 3-(cyanomethoxy)acrylates, using aldehydes as substrates, acetone cyanohydrin as the cyanide anion source, and methyl propiolate as the source of the vinyl component. The multicomponent reaction is catalyzed by -methyl morpholine (2.5 mol%) to deliver the 3-(cyanomethoxy)acrylates in excellent yields and with preponderance of the -isomer. The multicomponent reaction manifold is highly tolerant to the structure and composition of the aldehyde (aliphatic, aromatic, heteroaromatics), and it is instrumentally simple (one batch, open atmospheres), economic (2.5 mol% catalyst, stoichiometric reagents), environmentally friendly (no toxic waste), and sustainable (easy scalability).
设计了一种新颖的醛的有机催化多组分氰乙烯化反应,用于合成共轭氰甲基乙烯基醚。该反应以醛为底物,丙酮氰醇为氰阴离子源,丙炔酸甲酯为乙烯基组分来源,用于合成 3-取代的 3-(氰甲氧基)丙烯酸酯。该多组分反应由 -甲基吗啉(2.5mol%)催化,以优异的收率和优势的 -异构体得到 3-(氰甲氧基)丙烯酸酯。多组分反应方式对醛的结构和组成具有很高的耐受性(脂肪族、芳香族、杂环芳香族),且仪器操作简单(一批、开放气氛)、经济(2.5mol%催化剂、化学计量试剂)、环保(无有毒废物)和可持续(易于扩大规模)。