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One-Pot Synthesis of Secondary Amines from Nitroarenes and Aldehydes on Supported Copper Catalysts in a Flow Reactor: The Effect of the Support Научная публикация

Журнал Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Вых. Данные Год: 2018, Том: 59, Номер: 5, Страницы: 593-600 Страниц : 8 DOI: 10.1134/s0023158418050014
Ключевые слова one-stage synthesis, secondary amines, nitroarenes, aldehydes, flow reactor, molecular hydrogen, supported copper catalysts, support effect
Авторы Artyukha E.A. 1 , Nuzhdin A.L. 1 , Bukhtiyarova G.A. 1 , Derevyannikova E.A. 1 , Gerasimov E.Yu. 1 , Gladkii A.Yu. 1 , Bukhtiyarov V.I. 1,2
Организации
1 Boreskov Institute of Catalysis, Siberian Branch, Russian Academy of Sciences, Novosibirsk, 630090 Russia
2 Novosibirsk State University, Novosibirsk, 630090 Russia

Информация о финансировании (1)

1 Федеральное агентство научных организаций России 0303-2016-0006 (V.44.1.6)

Реферат: The effect of the support on the properties of copper catalysts supported on γ-Al2O3, SiO2, and TiO2–SiO2 with a ~5 wt % Cu content was studied in the one-pot synthesis of N-heptyl-p-toluidine from p-nitrotoluene and n-heptanal. The catalysts were characterized by elemental analysis, X-ray diffraction analysis, transmission electron microscopy, temperature-programmed reduction, and low-temperature nitrogen adsorption. The reaction was carried out in a flow reactor with the use of molecular hydrogen as a reducing agent. It was established that the nature of the support exerts a profound effect on the yield of the target secondary amine; in this case, 5%Cu/Al2O3 was found the most active catalyst. A combination of high catalyst activity in the hydrogenation of a nitro group to an amino group with the presence of acid sites, which facilitate imine formation as a result of the interaction of n-heptanal with p-toluidine, on the catalyst surface is necessary for reaching the greatest yield of N-heptyl-p-toluidine. The study of reaction mechanism on the 5%Cu/Al2O3 catalyst showed that p-nitrotoluene inhibits the hydrogenation of n-heptanal, and aldehyde hydrogenation into alcohol begins only after the conversion of the major portion of p-nitrotoluene as a result of the selective adsorption of the nitroarene under the conditions of the simultaneous presence of p-nitrotoluene and n-heptanal in the reaction mixture.
Библиографическая ссылка: Artyukha E.A. , Nuzhdin A.L. , Bukhtiyarova G.A. , Derevyannikova E.A. , Gerasimov E.Y. , Gladkii A.Y. , Bukhtiyarov V.I.
One-Pot Synthesis of Secondary Amines from Nitroarenes and Aldehydes on Supported Copper Catalysts in a Flow Reactor: The Effect of the Support
Kinetics and Catalysis. 2018. V.59. N5. P.593-600. DOI: 10.1134/s0023158418050014 WOS Scopus РИНЦ CAPlusCA OpenAlex
Оригинальная: Артюха Е.А. , Нуждин А.Л. , Бухтиярова Г.А. , Деревянникова Е.А. , Герасимов Е.Ю. , Гладкий А.Ю. , Бухтияров В.И.
Одностадийный синтез вторичных аминов из нитроаренов и альдегидов на нанесенных медных катализаторах в проточном реакторе: влияние носителя
Кинетика и катализ. 2018. Т.59. №5. С.583-590. DOI: 10.1134/S0453881118050015 РИНЦ OpenAlex
Даты:
Поступила в редакцию: 1 мар. 2018 г.
Опубликована в печати: 1 сент. 2018 г.
Опубликована online: 26 сент. 2018 г.
Идентификаторы БД:
Web of science: WOS:000445762600008
Scopus: 2-s2.0-85053897737
РИНЦ: 35736802
Chemical Abstracts: 2018:1804581
Chemical Abstracts (print): 170:586507
OpenAlex: W2892624216
Цитирование в БД:
БД Цитирований
Web of science 11
Scopus 12
РИНЦ 11
OpenAlex 12
Альметрики: