262
Views
7
CrossRef citations to date
0
Altmetric
Research Articles

The Eggshell Waste Transformed Green and Efficient Synthesis of K-Ca(OH)2 Catalyst for Room Temperature Synthesis of Chalcones

, , , &
Pages 1322-1340 | Received 23 Feb 2020, Accepted 27 May 2020, Published online: 11 Jun 2020

References

  • Z. Li, H. Zhao, H. Han, Y. Liu, J. Song, W. Guo, W. Chu, and Z. Sun, “Graphene Supported ZnO Nanoparticles: An Efficient Heterogeneous Catalyst for the Claisen–Schmidt Condensation Reaction without Additional Base,” Tetrahedron Letters 58, no. 42 (2017): 3984–8.
  • J. N. Domínguez, C. León, J. Rodrigues, N. Gamboa de Domínguez, J. Gut, and P. J. Rosenthal, “Synthesis and Evaluation of New Antimalarial phenylurenyl chalcone derivatives,” Journal of Medicinal Chemistry 48, no. 10 (2005): 3654–8.
  • M. Marder and A. C. Paladini, “GABA(A)-Receptor Ligands of Flavonoid Structure,” Current Topics in Medicinal Chemistry 2, no. 8 (2002): 853–67.
  • F. Orallo, “Trans-Resveratrol: A Magical Elixir of Eternal Youth,” Current Medicinal Chemistry 15, no. 19 (2008): 1887–98.
  • A. Modzelewska, C. Pettit, G. Achanta, N. Davidson, P. Huang, and S. Khan, “Anticancer Activities of Novel Chalcone and Bis-Chalcone Derivatives,” Bioorganic & Medicinal Chemistry 14, no. 10 (2006): 3491–5.
  • K. Kunimasa, S. Kuranuki, N. Matsuura, N. Iwasaki, M. Ikeda, A. Ito, Y. Sashida, Y. Mimaki, M. Yano, M. Sato, et al. “Identification of Nobiletin, a Polymethoxyflavonoid, as an Enhancer of Adiponectin Secretion,” Bioorganic & Medicinal Chemistry Letters 19, no. 7 (2009): 2062–4.
  • M. Kawai, T. Hirano, J. Arimitsu, S. Higa, Y. Kuwahara, K. Hagihara, Y. Shima, M. Narazaki, A. Ogata, M. Koyanagi, et al. “Effect of Enzymatically Modified Isoquercitrin, a Flavonoid, on Symptoms of Japanese Cedar Pollinosis: A Randomized Double-Blind Placebo-Controlled Trial,” International Archives of Allergy and Immunology 149, no. 4 (2009): 359–68.
  • M. Sazegar, S. Mahmoudian, A. Mahmoudi, S. Triwahyono, A. Jalil, R. Mukti, N. Kamarudin, and M. Ghoreishi, “Catalyzed Claisen–Schmidt Reaction by Protonated Aluminate Mesoporous Silica Nanomaterial Focused on the (E)-Chalcone Synthesis as a Biologically Active Compound,” RSC Advances 6, no. 13 (2016): 11023–31.
  • S. Nielsen, S. Christensen, G. Cruciani, A. Kharazmi, and T. Liljefors, “Antileishmanial Chalcones: Statistical Design, Synthesis, and Three-Dimensional Quantitative Structure-Activity Relationship Analysis,” Journal of Medicinal Chemistry 41, no. 24 (1998): 4819–32.
  • X. Bu and Y. Li, “Synthesis of Exiguaflavanone K and (±)-Leachianone G,” Journal of Natural Products 59, no. 10 (1996): 968–9.
  • L. J. Mazza and A. Guarna, “An Improved Synthesis of 1,3-Diphenyl-2-Buten-1-Ones (β-Methylchalcones),” Synthesis 1980, no. 1 (1980): 41–4.
  • R. S. Varma, G. W. Kabalka, L. T. Evans, and R. M. Pagni, “Aldol Condensations on Basic Alumina: The Facile Syntheses of Chalcones and Enones in a Solvent-Free Medium,” Synthetic Communications 15, no. 4 (1985): 279–84.
  • G. V. Reddy, D. Maitraie, B. Narsaiah, Y. Rambabu, and P. S. Rao, “Microwave Assisted Knoevenagel Condensation: A Facile Method for the Synthesis of Chalcones,” Synthetic Communications 31, no. 18 (2001): 2881–4.
  • M. Kantam, V. Prakash, and C. Reddy, “Efficient Synthesis of Chalcones by a Solid Base Catalyst,” Synthetic Communications 35 (2005): 1971–8.
  • M. Drexler and M. Amiridis, “The Effect of Solvents on the Heterogeneous Synthesis of Flavanone over MgO,” Journal of Catalysis 214, no. 1 (2003): 136–45.
  • B. Choudary, K. Ranganath, J. Yadav, and M. Kantam, “Synthesis of Flavanones Using Nanocrystalline MgO,” Tetrahedron Letters 46, no. 8 (2005): 1369–71.
  • S. Kumar, M. S. Lamba, and J. K. Makrandi, “An Efficient Green Procedure for the Synthesis of Chalcones Using C-200 as Solid Support under Grinding Conditions,” Green Chemistry Letters and Reviews 1, no. 2 (2008): 123–5.
  • A. Alcantara, J. Marinas, and J. Sinisterra, “Synthesis of 2′-Hydroxychalcones and Related Compounds in Interfacial Solid-Liquid Conditions,” Tetrahedron Letters 28, no. 14 (1987): 1515–8.
  • M. Climent, A. Corma, S. Iborra, and J. Primo, “Base Catalysis for Fine Chemicals Production: Claisen–Schmidt Condensation on Zeolites and Hydrotalcites for the Production of Chalcones and Flavanones of Pharmaceutical Interest,” Journal of Catalysis 151, no. 1 (1995): 60–6.
  • S. Sebti, A. Solhy, R. Tahir, S. Boulaajaj, J. Mayoral, J. Fraile, A. Kossir, and H. Oumimoun, “Calcined Sodium Nitrate/Natural Phosphate: An Extremely Active Catalyst for the Easy Synthesis of Chalcones in Heterogeneous Media,” Tetrahedron Letters 42, no. 45 (2001): 7953–5.
  • N. Iranpoor and F. Kazemi, “RuCl3 Catalyses Aldol Condensations of Aldehydes and Ketones,” Tetrahedron Letters 54, no. 32 (1998): 9475–80.
  • Z. N. Siddiqui, “A Convenient Synthesis of Coumarinyl Chalcones Using HClO4-SiO2: A Green Approach,” Arabian Journal of Chemistry 15 (2015): 00184–7.
  • D. Oliveira, P. Benelli, and E. Amante, “A Literature Review on Adding Value to Solid Residues: Egg Shells,” Journal of Cleaner Production 46 (2013): 42–7.
  • D. Kumar and A. Ali, “Nanocrystalline K–CaO for the Transesterification of a Variety of Feedstocks: Structure, Kinetics and Catalytic Properties,” Biomass and Bioenergy 46, (2012): 459–68.
  • B. Shinde, S. Kamble, D. Pore, P. Gosavi, A. Gaikwad, H. Jadhav, B. Karale, and A. Burungale, “pH-Transformed ZnO-NPs/NaPTS: The First Room-Temperature Brisk Synthesis of Flavanones in Aqueous Medium,” ChemistrySelect 3, no. 46 (2018): 13197–206.
  • K. Elumalai, S. Velmurugan, S. Ravi, V. Kathiravan, and S. Ashokkumar, “Green Synthesis of Zinc Oxide Nanoparticles Using Moringa oleifera Leaf Extract and Evaluation of Its Antimicrobial Activity,” Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy 143 (2015): 158–64.
  • X. Li, B. Wang, X. Cai, W. Yu, L. Zhang, G. Wang, and S. Ke, “Arsenene/CaOH2 Van Der Waals Heterostructure: Strain Tunable Electronic and Photocatalytic Properties,” RSC Advances 7, no. 70 (2017): 44394–400.
  • M. Ghiasi and A. Malekzadeh, “Synthesis of CaCO3 Nanoparticles via Citrate Method and Sequential Preparation of CaO and Ca(OH)2 Nanoparticles,” Crystal Research and Technology 47, no. 4 (2012): 471–8.
  • T. Liu, Y. Zhu, X. Zhang, T. Zhang, T. Zhang, and X. Li, “Synthesis and Characterization of Calcium Hydroxide Nanoparticles by Hydrogen Plasma-Metal Reaction Method,” Materials Letters 64, no. 23 (2010): 2575–7.
  • A. Roy and J. Bhattacharya, “Microwave-Assisted Synthesis and Characterization of CaO Nanoparticles,” International Journal of Nanoscience 10, no. 3 (2011): 413–8.
  • Z. Mirghiasi, F. Bakhtiari, E. Darezereshki, and E. Esmaeilzadeh, “Non-Isothermal Kinetic and Thermodynamic Studies of the Dehydroxylation Process of Synthetic Calcium Hydroxide Ca(OH)2,” Journal of Industrial and Engineering Chemistry 20, no. 1 (2014): 113–7.
  • E. Darezereshki, “Synthesis of Maghemite (γ-Fe2O3) Nanoparticles by Wet Chemical Method at Room Temperature,” Materials Letters 64, no. 13 (2010): 1471–2.
  • P. Lagarde, M. A. H. Nerenberg, and Y. Lagarde, “Ca(OH)2 Infrared Vibrational Spectra around 3600 cm−1 Experimental and Theoretical Study on Microcrystals and Single Crystals,” Physical Review B 8, no. 4 (1973): 1731–46.
  • B. Salvadori and L. Dei, “Synthesis of Ca(OH)2 Nanoparticles from Diols,” Langmuir 17, no. 8 (2001): 2371–4.
  • M. Lejodi, D. Waal, J. Potgieter, and S. Potgieter, “Rapid Determination of CaCO3 in Mixtures Utilising FT-IR Spectroscopy,” Minerals Engineering 14 (2001): 1107–11.
  • D. Breslow and C. Hauser, “Condensations. XI. Condensations of Certain Active Hydrogen Compounds Effected by Boron Trifluoride and Aluminum Chloride,” Journal of the American Chemical Society 62, no. 9 (1940): 2385–8.
  • S. Sarda, W. Jadhav, S. Tekale, G. Jadhav, B. Patil, G. Suryawanshi, and R. Pawar, “Phosphonium Ionic Liquid Catalyzed an Efficient Synthesis of Chalcones,” Letters in Organic Chemistry 6, no. 6 (2009): 481–4.
  • D. Dhar and J. Lal, “Chalcones. Condensation of Aromatic Aldehydes with Resacetophenone,” The Journal of Organic Chemistry 23, no. 8 (1958): 1159–61.
  • N. Calloway and L. Green, “Reactions in the Presence of Metallic Halides. I. β-Unsaturated Ketone Formation as a Side Reaction in Friedel–Crafts Acylations,” Journal of the American Chemical Society 59, no. 5 (1937): 809–11.
  • A. Fuentes, J. Marinas, and J. Sinisterra, “Catalyzed Synthesis of Chalcones under Interfacial Solid-Liquid Conditions with Ultrasound,” Tetrahedron Letters 28, no. 39 (1987): 4541–4.
  • J.-T. Li, W.-Z. Yang, S.-X. Wang, S.-H. Li, and T.-S. Li, “Improved Synthesis of Chalcones under Ultrasound Irradiation,” Ultrasonics Sonochemistry 9, no. 5 (2002): 237–9.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.