RUS  ENG
Полная версия
ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 2024, том 34, выпуск 1, страницы 116–118 (Mi mendc60)

Эта публикация цитируется в 1 статье

Communications

An efficient synthesis of substituted 4,5-dihydroxyimidazolidin-2-ones by oxidation of imidazolin-2-ones with HNO3

V. V. Baranova, P. D. Prakhovab, N. G. Kolotyrkinaa, A. N. Kravchenkoa

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b D.Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation


Аннотация: Previously unavailable 1,3-dialkyl-4,5-diaryl-4,5-dihydroxyimidazolidin-2-ones were obtained by the oxidation of 1,3-dialkyl-4,5-diaryl-4-imidazolin-2-ones with HNO3 (65 or 84% aq.). The scope of required 4-imidazolin-2-ones obtained from acyloins has been expanded, which provided preparation of new representatives of the title compounds.

Ключевые слова: 4,5-dihydroxyimidazolidin-2-ones, nitric acid, oxidation, 4-imidazolin-2-ones, diastereomers, acyloins, ureas.

Язык публикации: английский

DOI: 10.1016/j.mencom.2024.01.035



© МИАН, 2025