New adducts of turpentine and rosin with citraconic anhydride and itaconic acid
https://doi.org/10.29235/1561-8331-2018-54-4-434-441
Abstract
The reaction of pine gum rosin, turpentine and its components (α-pinene, ∆3-carene, α-terpinene) with citraconic anhydride and itaconic acid was investigated. It was shown that α-terpinene, in contrast to α-pinene and ∆3-carene, reacts with citraconic anhydride to give the unknown cycloaddition reaction product. Its structure was studied by the 2D NMR spectroscopy. Turpentine reacts with itaconic acid forming a complex mixture that contains esters of terpenic alcohols and itaconic acid. Reaction of rosin with citraconic anhydride was studied at 140–180 °С within 0.5–8 hrs in presence of catalytic amounts of H2SO4, MgCl2, AlCl3, FeCl3 and new citraconopimaric adducts containing up to ~70 % of citraconopimaric acid as a mixture of two С15–CH3 and С16–CH3 isomers in equimolar ratio. The highest content of С15–CH3 isomer of citraconopimaric acid (35.5–36.0 %) in the adducts was reached within 4–8 hrs at 180 °С in presence of 1–2 mass. % H2SO4. The reaction of rosin with citraconic anhydride at 140–160 °С leads to the formation of adduct containing up to 30–50 % of citraconopimaric acid isomers. The synthesized adducts may be used for production of composite materials for different applications (adhesives, polymer composite additives including rubber blends for tire production, components of grease-cooling liquids).
About the Authors
M. P. BeiBelarus
Ph. D (Сhemistry), Senior researcher
N. V. Puchkova
Belarus
Junior researcher
A. P. Yuvchenko
Belarus
Ph. D (Сhemistry), Senior researcher, Deputy Director
A. V. Baranovsky
Belarus
D. Sc. (Сhemistry), Head of the Laboratory
References
1. Panda H. Handbook on Oleoresin and Pine Chemicals. Asia Pacific Business Press, 2008. 608 p.
2. Radbil’ A. B. Directions for the qualified use of turpentine. Khimija rastitel’nogo syr’ ja = Chemistry of plant raw material, 2005, no 1, pp. 5–11 (in Russian).
3. Pronevich A. N. Preparation, properties and application of terpenomaleated resins. Ph. D tech. sci. diss. thesis. Minsk, 1999. 22 p. (in Russian).
4. Klyuev A. Yu., Skakovskii E. D., Kozlov N. G., Pronevich A. N., Prokopchuk N. R., Udarov B. G. Terpenoid maleic adducts and their derivatives: synthesis, properties and application. Sbornik nauchnyh trudov: Himia i technologia novyh veshchestv i materialov [Proceedings: Chemistry and Technology of new substances and materials]. Minsk, 2008, no. 2, pp. 374–419 (in Russian).
5. Kuenz A., Krull S. Biotechnological production of itaconic acid – things you have to know. Applied Microbiology and Biotechnology, 2018, vol. 102, no. 9, pp. 3901−3914. https://doi.org/10.1007/s00253-018-8895-7
6. Marshall H. Preparation of citraconic anhydride. Patent USA, no. 5491215, 1960.
7. Bei M. P., Yuvchenko A. P. The method for preparation of citraconopimaric acid. Patent Republic of Belarus, no. 13646, 2010 (in Russian).
8. Yuan Mei Nie, Kun Gang Chai, Zhan Wan Shi, Xing Dong Yao. Investigation on the Synthesis of α-Terpinene and Maleic Anhydride Adduct Catalyzed by Heteropolyacid. Advanced Materials Research, 2012, vol. 361–363, pp. 1063–1065. https:// doi.org/10.4028/www.scientific.net/amr.361-363.1063.
9. Da Silva Rocha K. A., Robles-Dutenhefner P. A., Kozhevnikov I. V., Gusevskaya E. V. Phosphotungstic heteropoly acid as efficient heterogeneous catalyst for solvent-free isomerization of α-pinene and longifolene. Applied Catalysis A: General, 2009, vol. 352, no. 1–2, pp. 188–192. https://doi.org/10.1016/j.apcata.2008.10.005.
10. Derome A. E. Modern NMR Techniques for Chemistry Research. Oxford: Pergamon Press, 1987. 280 p. https:// doi.org/10.1016/c2009-0-07888-x
11. Shkapova Yu. A., Radbil’ A. B., Zolin B. A., Radbil’ B. A. Reaction of α-Pinene with Haloacetic Acids. Russian Journal of Applied Chemistry, 2002, vol. 75, no. 2, pp. 310–314. https://doi.org/10.1023/a:1016185024931
12. Skakovskii E. D., Tychinskaya L. Yu., Gaidukevich O. A., Kozlov N. G. , Klyuev A. Yu., Lamotkin S. A., Shpak S. I., Rykov S. V. NMR determination of the composition of balsams from scotch pine resin. Journal of Applied Spectroscopy, 2008, vol. 75, no. 3, pp. 439−443. https://doi.org/10.1007/s10812-008-9065-y
13. Gastambide B., Langlois L. Etudes stereochimiques VII. Syntheses dieniques en serie resinique; action des peroxoacides et des hydrures doubles. Helvetica Chimica Acta, 1968, vol. 51, no. 8, pp. 2048–2057. https://doi.org/10.1002/ hlca.19680510824
14. Vischnevskii K. V., Prokopchuk N. R., Bei M. P., Puchkova N. V., Yuvchenko A. P., Schkodich V. F. Some features of the properties of elastomer compositions with nitrogen-containing adducts of rosin. Vestnik Kazanskogo tekhnologicheskogo universiteta = Herald of Kazan Technological University, 2015, vol. 18, no. 2, pp. 2006–2009 (in Russian).