Kamble Sumit B, Swami Rameshwar K, Sakate Sachin S, Rode Chandrashekhar V
Chemical Engineering and Process Development Division, CSIR-National Chemical Laboratory, Dr. Homi Bhabha Road, Pune 411008 (India), Fax: (+91) 2590-2620.
Chempluschem. 2013 Nov;78(11):1393-1399. doi: 10.1002/cplu.201300248. Epub 2013 Oct 7.
A novel, nonleachable hybrid of heteropoly acid and polyvinylpyrrolidone (or povidone) catalyzes the acetalization of aldehydes in methanol at room temperature followed by reaction with indole to give bis(indolyl)methanes (BIMs) and tris(indolyl)methanes (TIMs) in quantitative yields (90-97 %). The catalyst was shown by pyridine FTIR spectroscopy to possess Brønsted acidity, and the hybrid formation was confirmed by XRD and P NMR studies. Friedel-Crafts alkylation of indole as well as the tandem synthesis of BIMs and TIMs were established with several types of carbonyl and indole substrates to give the corresponding products quantitatively. The catalyst was recycled efficiently for three successive runs without losing its original activity.
一种新型的、不可浸出的杂多酸与聚乙烯吡咯烷酮(或聚维酮)的杂化物,在室温下催化甲醇中醛的缩醛化反应,随后与吲哚反应,以定量产率(90 - 97%)生成双(吲哚基)甲烷(BIMs)和三(吲哚基)甲烷(TIMs)。吡啶傅里叶变换红外光谱表明该催化剂具有布朗斯台德酸性,X射线衍射和磷核磁共振研究证实了杂化物的形成。利用几种类型的羰基和吲哚底物实现了吲哚的傅克烷基化反应以及BIMs和TIMs的串联合成,以定量方式得到相应产物。该催化剂可有效循环使用三次,且不失其原始活性。