Ruthenium Silicate (RS-1) Zeolite: A New, as an Efficient and Recoverable Heterogeneous Catalyst for Knoevenagel Condensation.

Authors

  • Sachin P. Gadekar1, Ramdas N. Huse2 Nilam D. Bansode3, Machhindra K. Lande3#∗

Abstract

Ruthenium silicate zeolite catalyst was synthesized from tetraethyl ortho-silicate and ruthenium trichloride via simple co-precipitation method and hydrothermal technique and labeled as RS-1(Ruthenium silicate). The performed catalytic experiments revealed that RS-1 type zeolite catalyst had the high catalytic performance on the Knoevenagel condensation reactions, for instance, the conversion of 4-chlorobenzaldehyde and malononitrile into 2-(4-chlorobenzylidene)-malononitrile within a short reaction time." 

References

R.M. Kumbhare, M. Sridhar, Catal. Commun. 9, 403 (2008)

a) S. Mallouk, K. Bougrin, A. Laghzizil, R. Benhida, Molecules 15, 813 (2010) (b) C.D. Lind, C. Green, M. Bird, J.T.A. Jones, J.R. Riches, K.K. McKee, M.S. Sandford, D.A. Wakefield, C.M. Timperley, R. Soc. Open. Sci. doi.org/10.1098/rsos.140160, (c) R. Gupta, M. Gupta, S. Paul, R. Gupta, B. Kore, Chem. Soc. 30, 2419 (2009)

(a) P.S. Rao, R.V. Venkataratnam, Tetrahedron Lett 32, 5821 (1991), (b) H. Moison, F. Texier-Boullet, A. Foucaud, Tetrahedron 43, 537 (1987), (c) F. Texier-Boullet, A. Foucaud, Tetrahedron Letter 23, 4927 (1982) , (d) G. Dai, D. Shi, L. Zhou, Y. Huaxue, Chin. J. Appl. Chem. 12, 104 (1995), (e) J.A. Cabello, J.M. Campelo, A. Garcia, D. Luna, J.M. Marinas, J. Org. Chem. 49, 5195 (1984), (f) D. Prajapati, J.S. Sandhu, J Chem. Soc. Perkin. Trans. 1(1), 739 (1993), (g) W. Lehnert, Tetrahedron Lett. 54, 4723 (1970), (h) VSR R. Pullabhotla, A. Rahman, S.B. Jonnalagadda, Catal. Commun. 10, 365 (2009), (i) J. Bennazha, M. Zahouily, S. Sebti, A. Boukhari, E.M. Holt, Catal. Comun. 2, 101 (2001), (j) A. El Maadi, C.L. Matthiesen, P. Ershadi, J. Baker, D.M. Herron, E.M. Holt, J. Chem. Cryst. 33, 757 (2003), (k) S. Sebti, A. Smahi, A. Solhy, Tetrahedron Lett 43, 1813 (2002) , (l) S. Ernst, T. Bongers, C. Casel, S. Munsch, Stud Surf Sci Catal 125, 367, (1999), (m) Y.V.S. Rao, D.E. De Vos, P.A. Jacobs, J. Org. Chem. 64, 1033 (1999), (n) Q. Xu, B. Xu, H. Kong, P. He, J. Wang, T. Kannan, P. Ma, J. Wang J. Niu, Inorganic Chem. 59(15), 10665 (2020)

B.V. Lichitsky, A.A. Dudinov, M.M. Krayushkin, ARKIVOC (ix), 73 (2001)

E. Abdelghani, S.A. Said, M.G. Assy, A.M.A. Hamid, Arabian J. Chem. 10, S2926 (2017)

E. Abdelghani, W.S. Shehab, M. El-Mobayed, A.M.A. Hamid, Inter. J. Basic ppl. Sci. 1(3), 220 (2012)

G.M. Ziarani, A. Badiei, Z. Dashtianeha, P. Hajiabbasia, Rev. Roum. Chim. 58(9-10), 765 (2013)

J. Tiwari, M. Saquib, S. Singh, F. Tufail, M. Singh, J. Singh, J. Singh, Green Chem. 18, 3221 (2016)

K.D. Khalil, H.M. Al-Matar, Molecules 17, 12225 (2012)

M.S. Moustafa, S.M. Al-Mousawi, M.A. Selim, A.M. Mosallam, M.H. Elnagdi, Beilstein J. Org. Chem. 10, 141 (2014)

F. Tietze, N. Rackelmann, Pure Appl. Chem. 76, 1967 (2004)

F.J. Liang, Y.P, T. Kurata, J.K, H. Nishide, Polymer 46, 37679 (2005)

M. Zahouily, M. Salah, B. Bahlaouane, A. Rayadh, A. Houmam, E.A. Hamed, S. Sebti, Tetrahedron 60, 1631(2004)

K. Turpaev, M. Ermolenko, T. Cresteil, J.C. Drapier, Biochem Pharmacology Else. 82(5) (2011)

L. Jing, J. Wei, L. Zhou, Z. Huang, Z. Li, D. Wu, H. Xiang, X. Zhou, Chem. Eur. J. 16, 10955 (2010)

S.K. Mohamed, A.A. Abdelhamid, A.M. Maharramov, A.N. Khalilov, A.V. Gurbanovb, M.A. Allahverdiev, J. Chem. Pharma. Res. 4(3), 1787 (2012)

Published

2022-04-30

Issue

Section

Articles