Email this article Uncatalyzed Hydrodechlorination of Dichlorobiphenyls
- Authors: Gorbunova T.I.1, Pervova M.G.1, Saloutin V.I.1, Chupakhin O.N.1
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Affiliations:
- Postovskii Institute of Organic Synthesis, Ural Branch
- Issue: Vol 55, No 7 (2019)
- Pages: 988-990
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/220882
- DOI: https://doi.org/10.1134/S1070428019070121
- ID: 220882
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Abstract
Mono-, di-, and trichlorobiphenyls showed different reactivities toward alkali in 2-aminoethanol under reflux: 3-chlorobiphenyl remained unchanged, 2,4,5- and 2,4′,5-trichlorobiphenyls were completely converted to hydroxy derivatives, whereas 3,4-dichlorobiphenyl and a mixture of 2,4′-, 3,4′-, and 4,4′-dichlorobiphenyls gave rise to chlorobiphenyls in addition to hydroxybiphenyls.
About the authors
T. I. Gorbunova
Postovskii Institute of Organic Synthesis, Ural Branch
Author for correspondence.
Email: gorbunova@ios.uran.ru
Russian Federation, Yekaterinburg
M. G. Pervova
Postovskii Institute of Organic Synthesis, Ural Branch
Email: gorbunova@ios.uran.ru
Russian Federation, Yekaterinburg
V. I. Saloutin
Postovskii Institute of Organic Synthesis, Ural Branch
Email: gorbunova@ios.uran.ru
Russian Federation, Yekaterinburg
O. N. Chupakhin
Postovskii Institute of Organic Synthesis, Ural Branch
Email: gorbunova@ios.uran.ru
Russian Federation, Yekaterinburg
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