Application of Silica Supported Aluminium Hydroxide as a Low Cost Green Catalyst for the One Pot MCR Sythesis via Thermal Method
Abstract
The catalysis is the first and active side they are good yield with good reusability. The sequence of time. They are the time of reaction is smaller, it saves the energy and time consummation, another thing is the good catalyst is intelligent for the dynamic yield but are focused on the design the catalyst they have good effectiveness as well as good reusability with green chemistry concept. In today times much, research is being carried out on Nano particles green catalysis we have eco-friendly make an endeavoured for designing new catalyst from waste aluminium foil to new catalyst. So our catalyst is designed from waste aluminium foil and transformed into good and reusability catalyst. They are continuing produced the same yield up to 7-8 reaction cycle.
Keywords: ketone, Aromatic aldehydes & ammonium hydroxide hydrochloride, green path with help of silica supported catalyst.
DOI
https://doi.org/10.22270/jddt.v9i4-s.3161References
Facile, eco-friendly and one-pot synthesis of 3,4-disubstitutedisoxazol- 5(4H)-ones using starch solution as a reaction mediaRH Vekariya, HD Patel - 2017 - nopr.niscair.res.in
N Hazeri, MT Maghsoodlou, F Mir, M Kangani; An efficient one-pot three-component synthesis of tetrahydrobenzo [b] pyran and 3, 4-dihydropyrano [c] chromene derivatives using starch solution as catalyst Chinese Journal of …, 2014 - Elsevier
Kumari, M Rajeswari, JM Khurana , A Green Approach for the Synthesis of Novel 7, 11-Dihydro-6H-chromeno [3, 4-e] isoxazolo [5, 4-b] pyridin-6-one Derivatives Using Acidic Ionic Liquid [C4mim][HSO4]S - Australian Journal of Chemistry, 2016 - CSIRO
DABCO as a mild and efficient catalyst for the synthesis of tetrahydropyrimidines N Foroughifar, A Mobinikhaledi, B Rabeie, L Jalili - Rev Roum Chim, 2013 - revroum.lew.ro
An efficient synthesis of stable phosphorus ylides derived from triphenylphosphine, dialkyl acetylenedicarboxylates, and an NH-AcidMT Maghsoodlou, N Hazeri , Sulfur, and Silicon, 2006 - Taylor & Francis
One-pot multicomponent synthesis of highly substituted piperidines using p-toluenesulfonic acid monohydrate as catalyst
SS Sajadikhah, MT Maghsoodlou, N Hazeri… - Monatshefte für Chemie …, 2012 - Springer
DABCO as a mild and efficient catalyst for the synthesis oftetrahydropyrimidinesN Foroughifar, A Mobinikhaledi, B Rabeie, L Jalili - Rev Roum Chim, 2013 - revroum.lew.ro
R Tayebee, MM Amini, M Ghadamgahi ; H5PW10V2O40/Pip-SBA-15: A novel reusable organic–inorganic hybrid material as potentLewisacid catalyst for one-pot solvent-free synthesisof3,4-dihydropyrimidinones Journal of Molecular …, 2013 - Elsevier
Safaei-Ghomi, J., Javidan, A., Ziarati, A. et al. J Nanopart Res (2015) 17: 338. https://doi.org/10.1007/s11051-015-3142-y
Zhu Y, Xie M, Dong S, Zhao X, Lin L, Liu X, Feng X (2011) Asymmetric cycloaddition of b, g-unsaturated a-ketoesters with electron-rich alkenes catalyzed by a chiral Er(OTf)3/N, N´-dioxide complex: highly enantioselective synthesis of 3,4-dihydro-2H-pyrans. Chem Eur J 17:8202–8208
Wag Y, Xin X, Liang Y, Lin Y, Duan H, Dong D (2009) N, N, N´, N´-tetramethylchloroformamidinium chloride-mediated cyclizations of β-oxo amides: facile and divergent one-pot synthesis of substituted 2H-pyrans, 4H-pyrans and pyridin-2(1H)-ones. Adv Synth Catal 351:2217–2223
Venkatesham A, Rao RS, Nagaiah K, Yadav JS, RoopaJones G, Basha SJ, Sridhar B, Addlagatta A (2012) Synthesis of new chromeno-annulated cis-fused pyrano[3,4-c]pyran derivatives via domino Knoevenagel-hetero-Diels-Alder reactions and their biological evaluation towards antiproliferative activity. Med Chem Commun 3:652–658
Saundane AR, Vijaykumar K, Vaijinath AV (2013) Synthesis of novel 2-amino-4-(5′-substituted 2′-phenyl-1H-indol-3′-yl)-6-aryl-4H-pyran-3-carbonitrile derivatives as antimicrobial and antioxidant agents. Bioorg Med Chem Lett 23:1978–1984
Safaei-Ghomi J, Shahbazi-Alavi H, Heidari-Baghbahadorani E (2014) SnO nanoparticles as an efficient catalyst for the one-pot synthesis of chromeno[2,3-b]pyridines and 2-amino-3,5-dicyano-6-sulfanyl pyridines. RSC Adv 4:50668–50677
Safaei-Ghomi J, Kalhor S (2015) A convenient synthesis of 2-aminocyclohex-1-ene-1-carboxylic esters by FeCl3/SiO2 nanoparticles as robust and efficient catalyst. Chin Chem Lett 26:735–738.
Patil SA, Wang J, Li XS, Chen JJ, Jones TS, Hosni-Ahmed A, Patil R, Seibel WL, Li W, Miller DD (2012) New substituted 4H-chromenes as anticancer agents. Bioorg Med Chem Lett 22:4458–4461.
Naeimi H, Rashid Z, Zarnani AH, Ghahremanzadeh R (2014) Nanocrystalline magnesium oxide: an efficient promoter and heterogeneous nano catalyst for the one-pot synthesis of pyrazolotriazoles in green medium. J Nanoparticle Res 16:2416
Kumar D, Reddy VB, Sharad S, Dube U, Kapur S (2009) A facile one-pot green synthesis and antibacterial activity of 2-amino-4H-pyrans and 2-amino-5-oxo-5,6,7,8-tetrahydro-4H-chromenes. Eur J Med Chem 44:3805–3809
Chen WB, Wu ZJ, Pei QL, Cun LF, Zhang XM, Yuan WC (2010) Highly enantioselective construction of spiro[4H-pyran-3,3′-oxindoles] through a Domino Knoevenagel/Michael/Cyclization sequence catalyzed by cupreine. Org Lett 12:3132–3135
Banerjee S, Horn A, Khatri H, Sereda G (2011) A green one-pot multicomponent synthesis of 4H-pyrans and polysubstituted aniline derivatives of biological, pharmacological, and optical applications using silica nanoparticles as reusable catalyst. Tetrahedron Lett 52:1878–1881
Maddila, Suresh; Jonnalagadda, Sreekantha B.; Gangu, Kranthi K.; Recent Advances in the Synthesis of Pyrazole Derivatives Using MulticomponentReactionsBottom of Form Current Organic Synthesis, Volume 14, Number 5, August 2017, pp. 634-653(20).
Maleki, A., Jafari, A.A.& Yousefi, S. JIRANCHEMSOC(2017) 14:1801.https://doi.org/10.1007/s13738-017-1120-
Published


How to Cite
Issue
Section
Authors who publish with this journal agree to the following terms:
- Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0). that allows others to share the work with an acknowledgment of the work's authorship and initial publication in this journal.
- Authors are able to enter into separate, additional contractual arrangements for the non-exclusive distribution of the journal's published version of the work (e.g., post it to an institutional repository or publish it in a book), with an acknowledgment of its initial publication in this journal.
- Authors are permitted and encouraged to post their work online (e.g., in institutional repositories or on their website) prior to and during the submission process, as it can lead to productive exchanges, as well as earlier and greater citation of published work (See The Effect of Open Access).