Get 20M+ Full-Text Papers For Less Than $1.50/day. Start a 14-Day Trial for You or Your Team.

Learn More →

Bis(aminomethylation) of dihydroxynaphthalenes

Bis(aminomethylation) of dihydroxynaphthalenes ISSN 00125008, Doklady Chemistry, 2015, Vol. 463, Part 1, pp. 178–180. © Pleiades Publishing, Ltd., 2015. Original Russian Text © E.E. Nifant’ev, P.V. Slitikov, E.N. Rasadkina, 2015, published in Doklady Akademii Nauk, 2015, Vol. 463, No. 2, pp. 172–174. CHEMISTRY a b a Corresponding Member of the RAS E. E. Nifant’ev , P. V. Slitikov , and E. N. Rasadkina Received February 6, 2015 DOI: 10.1134/S0012500815070046 among the latter are aminomethylation, which enable A preparatively convenient method for bis(ami nomethylation) of dihydroxynaphthalenes with the one to introduce one or several nitrogencontaining use of heterocyclic amines was proposed for the first substituents into molecule. time. The structure and physicochemical properties of Initial compounds used were two dihydroxynaph the obtained compounds were studied. The presence thalenes, one of which contains two hydroxy groups in of strong intramolecular hydrogen bonds in 2,7dihy the same benzene ring (1,3dihydroxynaphthalene (I)), droxynaphthalene derivatives was confirmed by IR while the other contains the same groups in different and H NMR spectroscopy. rings (2,7dihydroxynaphthalene (II)). At present, no literature data are available on the mono and bis(ami The development of convenient and accessible nomethylation) of 1,3dihydroxynaphthalene (I). The methods of synthesis of heterofunctionalized aromatic monomethylation of 2,7dihydroxynaphthalene http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Doklady Chemistry Springer Journals

Bis(aminomethylation) of dihydroxynaphthalenes

Nifant’ev, E.; Slitikov, P.; Rasadkina, E.
Doklady Chemistry , Volume 463 (1) – Aug 1, 2015
Download PDF
3 pages

Loading next page...
 
/lp/springer-journals/bis-aminomethylation-of-dihydroxynaphthalenes-ETkfvXRs9w

References (6)

Publisher
Springer Journals
Copyright
Copyright © 2015 by Pleiades Publishing, Ltd.
Subject
Chemistry; Chemistry/Food Science, general; Industrial Chemistry/Chemical Engineering
ISSN
0012-5008
eISSN
1608-3113
DOI
10.1134/S0012500815070046
Publisher site
See Article on Publisher Site

Abstract

ISSN 00125008, Doklady Chemistry, 2015, Vol. 463, Part 1, pp. 178–180. © Pleiades Publishing, Ltd., 2015. Original Russian Text © E.E. Nifant’ev, P.V. Slitikov, E.N. Rasadkina, 2015, published in Doklady Akademii Nauk, 2015, Vol. 463, No. 2, pp. 172–174. CHEMISTRY a b a Corresponding Member of the RAS E. E. Nifant’ev , P. V. Slitikov , and E. N. Rasadkina Received February 6, 2015 DOI: 10.1134/S0012500815070046 among the latter are aminomethylation, which enable A preparatively convenient method for bis(ami nomethylation) of dihydroxynaphthalenes with the one to introduce one or several nitrogencontaining use of heterocyclic amines was proposed for the first substituents into molecule. time. The structure and physicochemical properties of Initial compounds used were two dihydroxynaph the obtained compounds were studied. The presence thalenes, one of which contains two hydroxy groups in of strong intramolecular hydrogen bonds in 2,7dihy the same benzene ring (1,3dihydroxynaphthalene (I)), droxynaphthalene derivatives was confirmed by IR while the other contains the same groups in different and H NMR spectroscopy. rings (2,7dihydroxynaphthalene (II)). At present, no literature data are available on the mono and bis(ami The development of convenient and accessible nomethylation) of 1,3dihydroxynaphthalene (I). The methods of synthesis of heterofunctionalized aromatic monomethylation of 2,7dihydroxynaphthalene

Journal

Doklady Chemistry – Springer Journals

Published: Aug 1, 2015

There are no references for this article.