Synthesis and Isomer Composition of 2-Polyfluoroalkoxy-1,3,2-dioxaphospholanes and -phosphinanes
作者:N. K. Gusarova、S. I. Verkhoturova、S. N. Arbuzova、T. I. Kazantseva、A. I. Albanov、A. M. Nalibaeva、G. K. Bishimbaeva、K. A. Apartsin、V. V. Kireeva、B. A. Trofimov
DOI:10.1134/s107036321804014x
日期:2018.4
Polyfluoroalkanols readily reacted with 2-chloro-1,3,2-dioxaphospholanes and 2-chloro-1,3,2-dioxaphosphinanes in hexane in the presence of triethylamine (-10 to 25A degrees C, 5 h) to give 2-polyfluoroalkoxy-1,3,2- dioxaphospholanes and 2-polyfluoroalkoxy-1,3,2-dioxaphosphinanes in 48-72% yield. The products were found to exist as mixtures of cis and trans isomers with the trans isomer predominating for the phospholanes and cis isomer predominating for the phosphinanes according to the H-1, C-13, F-19, and P-31 NMR data.