A Facile One-Pot Synthesis of 1,2,3,4-Tetrahydroisoquinoline-1-carbonitriles via the Electrogenerated Cyanide Anions from Acetonitrile

The electrosynthesis of 1,2,3,4-tetrahydroisoquinoline-1-carbonitriles by acetonitrile reduction is a green and safe strategy to replace the traditional cyanation. Herein, we have obtained the 1,2,3,4-tetrahydroisoquinoline-1-carbonitrile in good yields by a simple reaction between dihydroisoquinolin-2-ium iodide and the electrogenerated acetonitrile formed under low temperature conditions, when a solution of dry acetonitrile is electrolyzed at a Carbon rod as cathode and a magnesium plate as anode in undivided cell. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim

Авторы
Sbei N. 1 , Titov A.A. 1 , Markova E.B. 2 , Elinson M.N.3 , Voskressensky L.G. 1
Журнал
Издательство
Wiley-Blackwell
Номер выпуска
15
Язык
Английский
Страницы
4493-4495
Статус
Опубликовано
Том
5
Год
2020
Организации
  • 1 Research Center: Molecular Design and Synthesis of Innovative Compounds for Medicine, Peoples' Friendship University of Russia(RUDN University), Moscow, Miklukho-Maklaya st https://twitter.com/UniversityRudn, 117198, Russian Federation
  • 2 Physical and Colloidal Chemistry Department, RUDN University Peoples' Friendship University of Russia (RUDN University), Moscow, Miklukho-Maklaya st, 117198, Russian Federation
  • 3 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect, 47, Moscow, Moscow, Russian Federation
Ключевые слова
1,2,3,4-tetrahydroisoquinoline-1-carbonitrile; cathodic reduction; cyanide anion; dihydroisoquinolin-2-ium iodide; electrochemical synthesis
Дата создания
02.11.2020
Дата изменения
02.11.2020
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/64826/
Поделиться

Другие записи