Polyaralkylation of primary aromatic amines with 6-hybroxy-2,4-dimethyl-1,3-benzodioxane

Polyaralkylation of primary aromatic amines with 6-hybroxy-2,4-dimethyl-1,3-benzodioxane Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 1983, Volume: 19, Number: 10, Pages: 1053-1056 Pages count : DOI: 10.1007/BF00505750

Authors

Denisov V. Ya. , Fokin E. P.

Affiliations

1	(Scopus) Keremovo State University, Keremovo, 650043
2	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

6-Hydroxy-2,4-dimethyl-1,3-benzodioxane is cleaved with opening of the 1,3-dioxane ring in a mixture of acetic and hydrochloric acids. The resulting hydroquinonecontaining fragments N-aralkylate the primary amines (aminoanthraquinone, p-nitroaniline, and p-aminoazobenzene) which are added to the reaction mixture to give the corresponding N-(polyethylidenehydroquinone)arylamines. © 1984 Plenum Publishing Corporation.

Denisov V.Y. , Fokin E.P.
Polyaralkylation of primary aromatic amines with 6-hybroxy-2,4-dimethyl-1,3-benzodioxane
Chemistry of Heterocyclic Compounds. 1983. V.19. N10. P.1053-1056. DOI: 10.1007/BF00505750 Scopus РИНЦ OpenAlex

Published print:

Oct 1, 1983

Scopus:	2-s2.0-34250135888
Elibrary:	30919338
OpenAlex:	W1991200711

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