“…Generally, Knoevenagel reactions are carried out by condensation of active methylene compounds with aldehydes using some organic bases with their salts as catalysts, including dimethylamino pyridine, piperidine, guanidine, ethylenediamine (Narsaiah et al, 2004;Han et al, 2008), and so on. Also, alternative protocols for Knoevenagel condensations catalyzed by Lewis acids such as ZnCl 2 (Shanthan Rao & Venkataratnam, 1991), CuCl 2 (Attanasi et al, 1983), TiCl 4 (Green et al, 1985), LaCl 3 (Narsaiah & Nagaiah, 2003), Mg(ClO 4 ) 2 (Bartoli et al, 2008) and various heterogeneous solid bases, including Zeolites (Saravanamurugan et al, 2006;Martns et al, 2008), sulfate-ion promoted Zirconia , clay (Bigi et al, 1999), and layered double hydroxides (LDHs) (Kantam et al, 2006) have been reported in literatures. However, many of those procedures required the use of large amount of organic solvents as reaction medium, long reaction time, harsh reaction conditions and had difficulties in the reuse of catalysts, which prompt chemical researchers for further development of more environmentally benign, efficient and operationally simple Knoevenagel protocols.…”