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Two-Step One-Pot Reductive Amination of Furanic Aldehydes Using CuAlOx Catalyst in a Flow Reactor Научная публикация

Журнал Molecules
ISSN: 1420-3049
Вых. Данные Год: 2020, Том: 25, Номер: 20, Номер статьи : 4771, Страниц : 7 DOI: 10.3390/molecules25204771
Ключевые слова reductive amination; 5-hydroxymethylfurfural; 5-acetoxymethylfurfural; Cu-based catalyst; Cu-Al mixed oxide; primary amines; imine hydrogenation; flow reactor
Авторы Nuzhdin Alexey L. 1 , Bukhtiyarova Marina V. 1 , Bukhtiyarov Valerii I. 1
Организации
1 Boreskov Institute of Catalysis SB RAS, 630090 Novosibirsk, Russia

Информация о финансировании (1)

1 Российский научный фонд
FWF Austrian Science Fund
20-43-05002

Реферат: Aminomethylhydroxymethylfuran derivatives are well known compounds which are used in the pharmaceutical industry. Reductive amination of 5-hydroxymethylfurfural (HMF) derived from available non-edible lignocellulosic biomass is an attractive method for the synthesis of this class of compounds. In the present study, the synthesis of N-substituted 5-(hydroxymethyl)-2-furfuryl amines and 5-(acetoxymethyl)-2-furfuryl amines was performed by two-step process, which includes the condensation of furanic aldehydes (HMF and 5-acetoxymethylfurfural) with primary amines in methanol on the first step and the reduction of obtained imines with hydrogen in a flow reactor over CuAlOx catalyst derived from layered double hydroxide on the second step. This process does not require isolation and purification of intermediate imines and can be used to synthesize a number of aminomethylhydroxymethylfurans in good to excellent yield.
Библиографическая ссылка: Nuzhdin A.L. , Bukhtiyarova M.V. , Bukhtiyarov V.I.
Two-Step One-Pot Reductive Amination of Furanic Aldehydes Using CuAlOx Catalyst in a Flow Reactor
Molecules. 2020. V.25. N20. 4771 :1-7. DOI: 10.3390/molecules25204771 WOS Scopus РИНЦ CAPlusCA PMID OpenAlex
Файлы: Полный текст от издателя
Даты:
Поступила в редакцию: 26 сент. 2020 г.
Опубликована в печати: 1 окт. 2020 г.
Принята к публикации: 15 окт. 2020 г.
Опубликована online: 17 окт. 2020 г.
Идентификаторы БД:
Web of science: WOS:000585575100001
Scopus: 2-s2.0-85093652296
РИНЦ: 45205218
Chemical Abstracts: 2020:2221445
Chemical Abstracts (print): 174:7750
PMID (PubMed): 33080807
OpenAlex: W3093254304
Цитирование в БД:
БД Цитирований
Scopus 20
Web of science 19
РИНЦ 19
OpenAlex 21
Альметрики: