A simple synthesis of benzofurans by acid-catalyzed domino reaction of salicyl alcohols with N-tosylfurfurylamine

A simple route to polysubstituted benzofurans based on the domino reaction of commercial or easily available salicyl alcohols with N-protected furfurylamine has been designed and developed. The reaction was found to proceed with reasonable yields under heating of substrates in acetic acid in the presence of catalytic amount of conc. HCl when tosyl was used as protecting group. © 2017 Elsevier Ltd

Авторы
Merkushev A.A.1, 2 , Strel'nikov V.N.2 , Uchuskin M.G. 1, 3 , Trushkov I.V. 3, 4
Журнал
Номер выпуска
46
Язык
Английский
Страницы
6523-6529
Статус
Опубликовано
Том
73
Год
2017
Организации
  • 1 Perm State University, Bukireva 15, Perm, 614990, Russian Federation
  • 2 Institute of Technical Chemistry UB RAS, Academica Koroleva 3, Perm, 614013, Russian Federation
  • 3 RUDN University, Miklukho-Maklaya 6, Moscow, 117198, Russian Federation
  • 4 Dmitry Rogachev National Research Center of Pediatric Hematology, Oncology and Immunology, Samory Mashela 1, Moscow, 117997, Russian Federation
Ключевые слова
Benzofurans; Bronsted acid catalysis; Domino reaction; Furan; Salicyl alcohols
Дата создания
19.10.2018
Дата изменения
28.09.2021
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/5179/
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