An Efficient One-Pot Synthesis of Phenol Derivatives by Ring Opening and Rearrangement of Diels-Alder Cycloadducts of Substituted Furans Using Heterogeneous Catalysis and Microwave Irradiation
作者:Andrés Moreno、Antonio de la Hoz、María Victoria Gómez、Ester Vázquez、Angel Díaz-Ortiz、Pilar Prieto、José Antonio Mayoral、Elisabet Pires
DOI:10.1055/s-2004-825604
日期:——
under microwave irradiation promotes regiospecific opening of the 7-oxa bridge of Diels-Alder cycloadducts of furan derivatives and produces polysubstituted phenols in a single step. This rapid and efficient procedure permits the synthesis of tri-, tetra- and pentasubstituted benzene derivatives by reaction of 2,5-dimethylfuran (1), 2-ethylfuran (2) and 2-methoxyfuran (3) with dienophiles such as dimethyl
在微波辐射下使用二氧化硅负载的路易斯酸作为催化剂促进了呋喃衍生物的 Diels-Alder 环加合物的 7-氧杂桥的区域特异性打开,并在一个步骤中产生多取代酚。这种快速有效的方法允许通过 2,5-二甲基呋喃 (1)、2-乙基呋喃 (2) 和 2-甲氧基呋喃 (3) 与亲二烯体(如乙炔二甲酸二甲酯和丙炔酸甲酯。