Transesterification of methyl salicylate with isoamyl alcohol assisted by microwave irradiation and promoted by acid-basic catalysts

References

• Irwin JW, Masuda QN, Li Wan Po A. Transesterification kinetics of phenyl salicylate. Tetrahedron. 1984;40:5217–5223.
   Google Scholar
• Amann R, Peskar BA. Anti-inflammatory effects of aspirin and sodium salicylate. Eur J Pharmacol. 2002;447:1–9.
   PubMed Web of Science ®Google Scholar
• Kokel A, Schafer C, Török B. Organic synthesis using environmentally benign acid catalysis. Curr Org Synth. 2019;16(4):615–649.
   PubMedGoogle Scholar
• Tajuddin NA, Lee AF, Wilson K. Handbook of biofuels production: processes and technologies, 2nd ed. Amsterdam (NL): Elsevier; 2016. Chapter 6: Production of biodiesel via catalytic upgrading and refining of sustainable oleagineous feedstocks. p. 121–164.
   Google Scholar
• Lotero E, Goodwin JG, Bruce DA, et al. The catalysis of biodiesel synthesis. Catalysis. 2006;19:41–83.
   Google Scholar
• Riemenschneider W, Bolt HM. Ullmann’s encyclopedia of industrial chemistry. Weinheim: Wiley-VCH; 2012. Volume 13, Esters, Organic. p. 245–265.
   Google Scholar
• Tao DJ, Wu J, Wang Z, et al. SO3H-functionalized Brønsted acidic ionic liquids as efficient catalysts for the synthesis of isoamyl salicylate. RSC Adv. 2014;4:1–7.
   Web of Science ®Google Scholar
• Shi H, Zhu W, Li H, et al. Microwave-accelerated esterification of salicylic acid using Brönsted acidic ionic liquids as catalysts. Catal Commun. 2010;11:588–591.
   Google Scholar
• Zhao Q, Chu J, Jiang T, et al. Synthesis of isoamyl salicylate using a novel mesoporous titania superacid as a catalyst. Korean J Chem Eng. 2008;25(5):1008–1013.
   Google Scholar
• Khokhar Z, Munir S, Haq EU, et al. Isoamyl salicylate: synthesis and use in beauty soap as a fragrance. Sci Int Lahore. 2011;23(2):121–124.
   Google Scholar
• Shyamsundar M, Shamshuddin SZM. Effective synthesis of n-butyl salicylate over wash coated cordierite honeycomb by zirconia and its mixed oxides: a kinetic study. Bangladesh J Sci Ind Res. 2018;53(1):63–76.
   Google Scholar
• Kumar TEM, Saritha SR, Shamshuddin SZM, et al. Synthesis of salicylate esters over cordierite honeycomb monoliths coated with zirconia based solid acids in vapour phase. Indian J Chem Technol. 2018;25:390–395.
   Google Scholar
• D’Souza J, Nagaraju N. Vapour phase transesterification over solid acids for the synthesis of isoamyl salicylate. Indian J Chem Technol. 2004;11:401–409.
   Web of Science ®Google Scholar
• Palma V, Barba D, Cortese M, et al. Microwaves and heterogeneous catalysis: a review on selected catalytic processes. Catalysts. 2020;10(2):246–305.
   Google Scholar
• Meredith R. Engineers’ handbook of industrial microwave heating: power and energy. London: The Institution of Electrical Engineers; 1998.
   Google Scholar
• Vogel AI. Vogel’s textbook of practical organic chemistry. London: Longman Scientific & Technical; 1989.
   Google Scholar
• Yang J, Guan Y, Verhoeven T, et al. Basic metal carbonate supported gold nanoparticles: enhanced performance in aerobic alcohol oxidation. Green Chem. 2009;11:322–325.
   Google Scholar
• Tanabe K, Misono M, Ono Y, et al. New solid acids and bases: their catalytic properties. Amsterdam: Elsevier; 1989.
   Google Scholar
• Take J, Kikuchi N, Yoneda Y. Base-strength distribution studies of solid-base surfaces. J Catal. 1971;21(2):164–170.
   Google Scholar
• Ren Y, Wu Z, Yang R, et al. A simple procedure for the esterification and transesterification using p-toluene sulfonic acid as catalyst. Adv Mat Research. 2013;781–784:259–262.
   Google Scholar
• Negm N, Betiha M, Alhumaimess M, et al. Clean transesterification process for biodiesel production using heterogeneous polymer-heteropoly acid nanocatalyst. J Cleaner Prod. 2019;328:117854.
   Google Scholar
• Bitonto L, Menegatti S, Patore C. Process intensification for the production of the ethyl esters of volatile fatty acids using aluminium chloride hexahydrate as a catalyst. J Cleaner Prod. 2019;239:118122.
   Google Scholar
• Calucci C, Degennaro L, Luisi R. Titanium dioxide as a catalyst in biodiesel production. Catalysts. 2019;9(75):1–25.
   Google Scholar
• Kim KS, Song SJ, Kim JH, et al. In situ generation of strong bases from alkaline and alkaline–earth carbonates. J Catalysis. 2002;205:244–247.
   Google Scholar
• Suppes G, Bockwinkel K, Lucas S, et al. Calcium carbonate catalyzed alcoholysis of fats and oils. JAOCS. 2001;78:139–146.
   Web of Science ®Google Scholar
• Dai YM, Lin JH, Huang ST, et al. Natural soil and lithium carbonate as economical solid-base catalysts for biodiesel production. Energy Rep. 2020;6:2743–2750.
   Google Scholar
• García-Raso A, Sinisterra JV, Marinas JM. A new barium hydroxide as a catalyst in organic synthesis. React Kinet Catal Lett. 1982;19:145–150.
   Google Scholar
• López Granados M, Zafra Poves M, Martín Alonso D, et al. Biodiesel from sunflower oil by using activated calcium oxide. Appl Catal B 2007;73:317–326.
   Web of Science ®Google Scholar
• Gouda M. LiOH.H2O as a catalyst for Knoevenagel and Gewald reactions. Pol J Chem Technol. 2010;12:31–35.
   Google Scholar
• Naik BD, Meivelu U. Experimental studies on sodium methoxide supportedbentonite catalyst for biodiesel preparation from wastesunflower oil. Environ Prog Sust Energy. 2020;39:1–14.
   PubMedGoogle Scholar
• Tanabe K, Misono M, Ono Y, et al. New solid acids and bases, Chapter 2. Kodansha: Elsevier; 1989.
   Google Scholar
• Levenspiel O. Chemical reaction engineering. New York: Wiley; 1999.
   Google Scholar
• Melo-Júnior CAR, Albuquerque MF, Dariva C, et al. Use of microwave irradiation in the noncatalytic esterification of C18 fatty acids. Energy Fuels. 2009;23:580–585.
   Google Scholar
• Wright MR. An introduction to chemical kinetics. London: Wiley; 2004.
   Google Scholar
• Castro CS, Ferretti C, Di Cosimo JI, et al. Support influence on the basicity promotion of lithium-based mixed oxides for transesterification reaction. Fuel. 2013;103:632–638.
   Web of Science ®Google Scholar
• Pasha M, Manjula K. Lithium hydroxide: A simple and an efficient catalyst for Knoevenagel condensation under solvent-free Grindstone method. J Saudi Chem Soc. 2011;15:283–286.
   Google Scholar