Abstract and keywords
Abstract (English):
V nastoyaschey rabote alkilirovaniem benzola geksanolom-1 sintezirovana smes', sostoyaschaya iz 60-65% 2-fenilgeksana i 35-40% 3 fenilgeksana. Issledovan perspektivnyy, no maloizuchennyy process aerobnogo zhidkofaznogo okisleniya dannoy smesi do sootvetstvuyuschih gidroperoksidov s cel'yu dal'neyshego polucheniya vysshih ketonov. Ustanovleno, chto ispol'zovanie na etoy stadii N gidroksiftalimida pozvolyaet dostich' tehnologicheskih pokazateley, priemlemyh dlya promyshlennoy realizacii. Tak, konversiya smesi fenilgeksanov sostavlyaet bolee 30% za 60 minut reakcii pri vysokoy selektivnosti obrazovaniya gidroperoksidov.

Keywords:
Alkilirovanie, okislenie, 2-fenilgeksan, 3-fenilgeksan
Text
Text (PDF): Read Download
References

1. Balakrishnan M., Arab G.E., Kunbargi O.B., Gokhale A.A., Grippo A.M., Toste F.D., Bell A.T. Production of renewable lubricants via self-condensation of methyl ketones. Green Chem., 2016, 18(12), 3577-3581. DOI:https://doi.org/10.1039/C6GC00579A.

2. Lopaschuk G.D., Dyck J.R. Ketones and the cardiovascular system. Nat. Cardiovasc. Res., 2023, 2(5), 425-437. DOI:https://doi.org/10.1038/s44161-023-00259-1. EDN: https://elibrary.ru/YBNJEJ

3. Albarracín Orio A.G., Petras D., Tobares R.A., Aksenov A.A., Wang M., Juncosa F., Sayago P., Moyano A.J., Dorrestein P.C., Smania A.M. Fungal-bacterial interaction selects for quorum sensing mutants with increased production of natural antifungal compounds. Commun. Biol., 2020, 3(1), 670. DOI:https://doi.org/10.1038/s42003-020-01342-0. EDN: https://elibrary.ru/BYZKJV

4. Gehrig R.F., Knight S.G. Formation of ketones from fatty acids by spores of Penicillium roqueforti. Nature, 1958, 182(4644), 1237-1237. DOI:https://doi.org/10.1038/1821237a0.

5. Fridman O.A. Plastifikaciya acetata cellyulozy. Izvestiya VUZov. Himiya i himicheskaya tehnologiya, 2010, 53(3), 82-86. EDN: https://elibrary.ru/OMQSSV

6. Tambovcev K.A., Yakovleva M.P., Ishmuratova N.M. Sinteticheskie feromonnye preparaty v pchelovodstve. Vestnik bashkirskogo universiteta, 2010, 15(2), 265-281. EDN: https://elibrary.ru/MSUBYJ

7. Karahanov E.A., Narin S.Yu., Filippova T.Yu., Dedov A.G. Pat. SU 1409621 A1, 1988.

8. Ulybin V.B., Efremov S.V., Romancova O.V. Sravnitel'nyy analiz razlichnyh metodov polucheniya peroksida vodoroda. Global'naya energiya, 2012, 3-2(154), 267-272. EDN: https://elibrary.ru/PESLKV

9. Knochel P., Molander G.A Comprehensive Organic Synthesis: Second Edition. Elsevier, 2014, 9806 p.

10. Elschenbroich C. Organometallics. Wiley-VCH: Weinheim, 2006, 804 p.

11. Stolyarov V.A. Novyy spravochnik himika i tehnologa. Syr'e i produkty promyshlennosti organicheskih i neorganicheskih veschestv. Ch. II. Sankt-Peterburg: ANO NPO “Professional”, 2005, 1141 s.

12. Rodikova Yu.A., Zhizhina E.G. Kataliticheskie metody polucheniya vysshih 2-ketonov: perspektivy Vaker-sistemy v reakcii okisleniya α-olefinov. Kin. i kat., 2023, 64(2), 121-138. DOI: https://doi.org/10.31857/S0453881123020065; EDN: https://elibrary.ru/GNRGKD

13. Gogin L.L. Rodikova Yu.A. Zhizhina E.G. Pat. RF 2790246 C1, 2023.

14. Shioyama T.K. Pat. USA 4507506, 1985.

15. Alper H., Januszkiewicz K., Smith D.J.H. A facile method for the amination of alkenes and other related reactions catalyzed by aluminum chloride. Tetrahedron Lett., 1985, 26(19), 2263-2266. DOI: https://doi.org/10.1016/S0040-4039(00)95069-X

16. Maksimov A.L., Buchneva T.S., Karahanov E.A. Okislenie olefinov do ketonov, kataliziruemoe vodorastvorimym kompleksom palladiya s kaliks[4]arenom, modificirovannym benzonitril'nymi gruppami. Neftehimiya, 2003, 43(3), 173-178. DOI: https://doi.org/10.1016/S0011-2275(03)00034-1; EDN: https://elibrary.ru/OOCUSL

17. Michel B.W., Sigman M.S. Peroxide-Mediated Wacker Oxidations for Organic Synthesis. Aldrichimica Acta, 2011, 44(3), 55-62.

18. Lai L., Pang H.W., Green W.H. Formation of two-ring aromatics in hexylbenzene pyrolysis. Energy Fuel, 2020, 34(2), 1365-1377. DOI:https://doi.org/10.1021/acs.energyfuels.9b03223. EDN: https://elibrary.ru/TQIAQW

19. Yarkina E.M., Kurganova E.A., Frolov A.S., Koshel' G.N., Nesterova T.N., Shakun V.A., Spiridonov S.A. Sintez para-tret-butilkumola. Tonkie himicheskie tehnologii, 2021, 16(1), 26-35. DOI: https://doi.org/10.32362/2410-6593-2020-16-1-26-35; EDN: https://elibrary.ru/NALYVK

20. Kabanova V.S., Kurganova E.A., Frolov A.S., Plahtinskiy V.V., Shakun V.A. Prognozirovanie kataliticheskoy aktivnosti ftalimidnyh soedineniy v processe zhidkofaznogo aerobnogo okisleniya alkilaromaticheskih uglevodorodov. Ot himii k tehnologii shag za shagom, 2024, 5(2), 8-16. DOI:https://doi.org/10.52957/2782-1900-2024-5-2-8-16. EDN: https://elibrary.ru/KIUKGS

21. Antonovskiy V.L., Buzlanova M.M. Analiticheskaya himiya organicheskih peroksidnyh soedineniy. M.: Himiya, 1978. 309 s.

22. Fox M.A., Whitesell J.K. Organic Chemistry. Sudbury, Mass.: Jones and Bartlett Publishers, 2003, 1140 p.

23. Song C.E., Shim W.H., Roh E.J., Choi J.H. Scandium(III) triflate immobilised in ionic liquids: a novel and recyclable catalytic system for Friedel-Crafts alkylation of aromatic compounds with alkenes. Chem. Commun., 2000, 17, 1695-1696. DOI:https://doi.org/10.1039/b005335j. EDN: https://elibrary.ru/AUKEAZ

24. Nel R.J., de Klerk A. Selectivity differences of hexene isomers in the alkylation of benzene over solid phosphoric acid. Ind. Eng. Chem. Res., 2007, 46(9), 2902-2906. DOI:https://doi.org/10.1021/ie061545q. EDN: https://elibrary.ru/XVAMUA

25. Bykov V.I., Belyaev B.A. Novyy sposob prigotovleniya katalizatorov alkilirovaniya na osnove geterogenizirovannogo AlCl3. Kin. i kat., 2021, 62(2), 277-280. DOI: https://doi.org/10.31857/S0453881121020027; EDN: https://elibrary.ru/JYGANN

26. Danilina N., Payrer E.L., Troussard E., van Bokhoven J.A. Selective Production of 2-Phenylhexane from Benzene and n-Hexane Over Pt- and Ga-Modified Zeolites. Catal. Lett., 2011, 141(3), 391-399. DOI:https://doi.org/10.1007/s10562-010-0511-0.

27. Alfa Aesar Research Chemical Metals and Materials. A Johnson Matthey Company, 2008, 2741 p.

28. Kurganova E.A., Baev E.I., Kabanova V.S., Frolov A.S., Koshel' G.N., Smurova A.A. Katalizatory processov okisleniya N-gidroksiftalimid i ego analogi. Neftegaz.ru, 2024, 5, 22-31. EDN: https://elibrary.ru/RHLOBO

Login or Create
* Forgot password?