Synthesis of polyfluoralkylated 1,3,2-dioxaphospholane and 1,3,2-dioxaphosphorinane oxides
- Authors: Gusarova N.K.1, Verkhoturova S.I.1, Arbuzova S.N.1, Kazantseva T.I.1, Albanov A.I.1, Nalibaeva A.M.2, Bishimbaeva G.K.2
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Affiliations:
- Favorskii Irkutsk Institute of Chemistry, Siberian Branch
- Institute of Fuel, Catalysis, and Electrochemistry
- Issue: Vol 53, No 11 (2017)
- Pages: 1623-1629
- Section: Article
- URL: https://journal-vniispk.ru/1070-4280/article/view/216892
- DOI: https://doi.org/10.1134/S107042801711001X
- ID: 216892
Cite item
Abstract
Polyfluoroalkyl dichlorophosphates easily react with 1,2- or 1,3-alkanediols in a system pyridine–diethyl ether and afford 2-polyfluoroalkoxy-1,3,2-dioxaphospholane oxides or 2-polyfluoroalkoxy-1,3,2-dioxaphosphorinane oxides. In similar conditions the reaction of methyl dichlorophosphate with 1,2- and 1,3-alkanediols proceeds less effectively.
About the authors
N. K. Gusarova
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Author for correspondence.
Email: gusarova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
S. I. Verkhoturova
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: gusarova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
S. N. Arbuzova
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: gusarova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
T. I. Kazantseva
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: gusarova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
A. I. Albanov
Favorskii Irkutsk Institute of Chemistry, Siberian Branch
Email: gusarova@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033
A. M. Nalibaeva
Institute of Fuel, Catalysis, and Electrochemistry
Email: gusarova@irioch.irk.ru
Kazakhstan, Almaty
G. K. Bishimbaeva
Institute of Fuel, Catalysis, and Electrochemistry
Email: gusarova@irioch.irk.ru
Kazakhstan, Almaty
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