Composition and reactivity of aminolysis products of phenyl glycidyl ether with benzylamine
- Authors: Pal’chikov V.A.1, Mykolenko S.Y.2, Pugach A.N.2, Zubkov F.I.3
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Affiliations:
- Oles’ Honchar Dnepropetrovsk National University
- Dnepropetrovsk State Agrarian and Economic University
- RUDN University
- Issue: Vol 53, No 5 (2017)
- Pages: 656-662
- Section: Article
- URL: https://bakhtiniada.ru/1070-4280/article/view/216172
- DOI: https://doi.org/10.1134/S1070428017050037
- ID: 216172
Cite item
Abstract
Composition of aminolysis products of phenyl glycidyl ether with benzylamine in various conditions was studied. The ratio of 1-(benzylamino)-3-phenoxypropan-2-ol and 1,1'-(benzylazanediyl)bis(3-phenoxypropan-2-ol) does not considerably depend on the nature of the solvent and is basically determined by ratio of initial reagents. 2,6-Bis(phenoxymethyl)morpholine was obtained by dehydration of aminodiol in conditions of Mitsunobu reaction with subsequent reductive debenzylation.
About the authors
V. A. Pal’chikov
Oles’ Honchar Dnepropetrovsk National University
Author for correspondence.
Email: palchikoff@mail.ru
Ukraine, pr. Gagarina 72, Dnepropetrovsk, 49010
S. Yu. Mykolenko
Dnepropetrovsk State Agrarian and Economic University
Email: palchikoff@mail.ru
Ukraine, Dnepropetrovsk
A. N. Pugach
Dnepropetrovsk State Agrarian and Economic University
Email: palchikoff@mail.ru
Ukraine, Dnepropetrovsk
F. I. Zubkov
RUDN University
Email: palchikoff@mail.ru
Russian Federation, Moscow
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