Oxidation of 4brometylbenzene by ozone in acetic acid
DOI:
https://doi.org/10.15587/1729-4061.2018.143207Keywords:
ozone-oxygen mixture, 4-bromethylbenzene, ozonolysis, 4-bromacetophenone, acetic acid, rate constantAbstract
The kinetics and the mechanism of ozonation of 4-bromethylbenzene in acetic acid was studied. The constants of the rate of reaction of ozone with 4-bromethylbenzene and 4-bromacetophenone at different temperatures were determined. We showed the possibility of conducting the process not only by the aromatic ring of the substrate in accordance with the Krige mechanism, but also with the formation of 4-bromacetophenone, which will be used when creating new methods of synthesis of oxygen-containing derivatives of ethylbenzene.
It was established that oxidation of 4-bromethylbenzene by ozone in acetic acid flows mainly by the aromatic ring with the formation of ozonides – peroxide products of aliphatic nature. Up to 35 % of 4-bromacetophenone and trace amounts of 1-(4-bromphenyl)ethanol were identified among the products of oxidation reaction by the side chain. The reaction of ozone with 4-bromethylbenzene in acetic acid at temperatures of up to30 °Chas the first order by initial components and the value of constant of reaction rate does not depend on the concentration of reactants. With increasing temperature, constant of reaction rate begins to depend on the concentration of reagents, and in this case, ozone consumption increases significantly. This indicates that under experimental conditions, ozone is consumed simultaneously at different stages of oxidation. It was proved that ozonation of 4-bromethylbenzene is a complicated process, in which the substrate is oxidized by the non-chain mechanism. Ozone is consumed in two directions: in the reaction with the substrate by non-chain mechanism and by the chain mechanism at the stage of chain continuation in the reaction with the products of thermal decomposition of ozonides. This fact gives grounds to argue that at an increase in temperature, unproductive consumption of ozone will grow rapidly and, vice versa, under conditions of prevention of ozonolysis, ozone will participate in the reaction with formation of the target aromatic product.
Thus, the experimentally obtained data are the basis for the development of the process of oxidation of derivatives of ethylbenzene and creation of the foundations of technology of 4-bromacetophenone synthesis with the help of ozone. This will considerably simplify the apparatus design of the process, enhance the output of the target product and will contribute to subsequent improvement of the method of oxidative processing of reagentsReferences
- Aleksandrov, V. N., Pugacheva, S. A., Golubev, G. S. (1980). Issledovanie reakcii okisleniya 4-nitrotoluola v uksusnoy kislote. Kinetika i kataliz, 21, 645.
- Emanuel', N. M. (1978). Problemy selektivnogo zhidkofaznogo okisleniya. Neftekhimiya, 18, 485.
- Okada, T., Kamiya, Y. (1981). The Liquid-phase Oxidation of Methylbenzenes by the Cobalt-Copper-Bromide System. Bulletin of the Chemical Society of Japan, 54 (9), 2724–2727. doi: https://doi.org/10.1246/bcsj.54.2724
- Di Nunno, L., Florio, S., Todesco, P. E. (1970). Oxidation of substituted anilines to nitroso-compounds. Journal of the Chemical Society C: Organic, 10, 1433. doi: https://doi.org/10.1039/j39700001433
- Yakobi, V. A. (1974). Gazofaznoe okislenie toluola ozonom. Neftekhimiya, 14, 399.
- Yakobi, V. A. (1976). Issledovanie processa hlorirovaniya α-sul'fokisloty antrahinona v prisutstvii ozona. Zhurn. prikl. himii, 49, 1330.
- A.S. No. 453404 SSSR (1973). Sposob polucheniya pirazol-3-karbonovoy kisloty. MKI S 07 s 46/12. declareted: 06.02.1973; published: 15.12.1974, Bul. No. 46.
- A.S. No. 480698 SSSR (1974). Sposob polucheniya 4-etilnaftalevogo angidrida. MKI S 07 s. declareted: 25.02.1974; published: 25.06.1975, Bul. No. 46.
- A.S. No. 330753 SSSR (1970). Sposob polucheniya tetrasernokislogo efira leykosoedineniya 7,16-dihlorindantrona. MKI S 09v 57/00. declareted: 16.03.1970; published: 23.02.1977, Bul. No. 45
- Digurov, N. G., Buharkina, T. V., Batygina, N. A. (1980). Matematicheskaya model' processa zhidkofaznogo okisleniya toluola i etilbenzola s kobal'tbromidnym katalizatorom. Kinetika i kataliz, 21 (3), 661–664.
- Bachernikova, I. V., Gorohovatskiy, Ya. B., Evmenenko, N. P. (1972). Zhidkofaznoe okislenie etilbenzola na okislah medi i nikelya. Neftekhimiya, 4, 563.
- Daniel, C. A., Sugunan, S. (2013). Ceria Zirconia Mixed Oxides Prepared by Hydrothermal Templating Method for the Oxidation of Ethyl Benzene. Bulletin of Chemical Reaction Engineering & Catalysis, 8 (2). doi: https://doi.org/10.9767/bcrec.8.2.5053.97-104
- Habibi, D., Faraji, A. R., Arshadi, M., Fierro, J. L. G. (2013). Characterization and catalytic activity of a novel Fe nano-catalyst as efficient heterogeneous catalyst for selective oxidation of ethylbenzene, cyclohexene, and benzylalcohol. Journal of Molecular Catalysis A: Chemical, 372, 90–99. doi: https://doi.org/10.1016/j.molcata.2013.02.014
- Mal, N. K., Ramaswamy, A. V. (1996). Oxidation of ethylbenzene over Ti-, V- and Sn-containing silicalites with MFI structure. Applied Catalysis A: General, 143 (1), 75–85. doi: https://doi.org/10.1016/0926-860x(96)00071-3
- Matienko, L. I., Mosolova, L. A. (2008). Effect of small concentrations of water on ethylbenzene oxidation with molecular oxygen catalyzed by iron(II, III) acetylacetonate complexes with 18-crown-6. Petroleum Chemistry, 48 (5), 371–380. doi: https://doi.org/10.1134/s0965544108050071
- Gavrichkov, A. A., Zakharov, I. V. (2005). Critical phenomena in ethylbenzene oxidation in acetic acid solution at high cobalt(II) concentrations. Russian Chemical Bulletin, 54 (8), 1878–1882. doi: https://doi.org/10.1007/s11172-006-0052-2
- Halstian, A. H., Kolbasiuk, O. O., Halstian, H. A., Bushuiev, A. S. (2013). The oxidation of ethylbenzene by ozone in acetic acid. Eastern-European Journal of Enterprise Technologies, 6 (6 (66)), 8–11. Available at: http://journals.uran.ua/eejet/article/view/18895/17125
- Solomatin, D. A., Halstian, A. H., Bushuiev, A. S., Kostenko, A. Yu. (2016). Ozonoliz 4-nitroetylbenzenu v otstoviy kysloti. Visnyk SNU im. V. Dalia, 5 (229), 19–22.
- Razumovskyi, S. D., Halstian, H. A., Tiupalo, M. F. (2000). Ozon ta yoho reaktsiyi z alifatychnymy spolukamy. Luhansk: SUDU, 318.
- Emanuelya, N. M. (1969). Uspekhi himii organicheskih perekisnyh soedineniy i autookisleniya. Moscow: Himiya, 495.
- Bailey, P. S. (1982). Ozonation in Organic Chemistry V2. Academic Press, 516.
- Emanuel', N. M., Denisov, E. T., Mayzus, Z. K. (1965). Cepnye reakcii okisleniya uglevodorodov v zhidkoy faze. Moscow: Nauka, 375.
- Pryor, W. A., Gleicher, G. J., Church, D. F. (1983). Reaction of polycyclic aromatic hydrocarbons with ozone. Linear free-energy relationships and tests of likely rate-determining steps using simple molecular orbital correlations. The Journal of Organic Chemistry, 48 (23), 4198–4202. doi: https://doi.org/10.1021/jo00171a008
- Avzyanova, E. V., Kabal'nova, N. N., Shereshovec, V. V. (1996). Kineticheskie zakonomernosti prevrashcheniya kompleksov ozona s arenami. Izv. RAN. Ser.: Him., 2, 371.
- Komissarov, V. D. (1979). Cepnoe razlozhenie ozona v sisteme CH3CHO-O3-O2. Izv. RAN. Ser.: Him., 6, 1205.
- Denisov, E. T., Mickevich, N. I., Agabekov, V. E. (1975). Mekhanizm zhidkofaznogo okisleniya kislorodsoderzhashchih soedineniy. Minsk: Nauka i tekhnika, 334.
- Bushuyev, A., Keremet, M., Galstyan, A., Galstyan, T. (2015). Kinetics and Products of 4-Aminotoluene Oxidization by Ozone in the Liquid Phase. Chemistry & Chemical Technology, 9 (1), 43–49. doi: https://doi.org/10.23939/chcht09.01.043
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2018 Andrew Galstyan, Ekaterina Skorokhod, Genry Galstyan
This work is licensed under a Creative Commons Attribution 4.0 International License.
The consolidation and conditions for the transfer of copyright (identification of authorship) is carried out in the License Agreement. In particular, the authors reserve the right to the authorship of their manuscript and transfer the first publication of this work to the journal under the terms of the Creative Commons CC BY license. At the same time, they have the right to conclude on their own additional agreements concerning the non-exclusive distribution of the work in the form in which it was published by this journal, but provided that the link to the first publication of the article in this journal is preserved.
A license agreement is a document in which the author warrants that he/she owns all copyright for the work (manuscript, article, etc.).
The authors, signing the License Agreement with TECHNOLOGY CENTER PC, have all rights to the further use of their work, provided that they link to our edition in which the work was published.
According to the terms of the License Agreement, the Publisher TECHNOLOGY CENTER PC does not take away your copyrights and receives permission from the authors to use and dissemination of the publication through the world's scientific resources (own electronic resources, scientometric databases, repositories, libraries, etc.).
In the absence of a signed License Agreement or in the absence of this agreement of identifiers allowing to identify the identity of the author, the editors have no right to work with the manuscript.
It is important to remember that there is another type of agreement between authors and publishers – when copyright is transferred from the authors to the publisher. In this case, the authors lose ownership of their work and may not use it in any way.