POLYFLUOROALKYLATION AND POLYFLUOROALKOXYLATION OF PERFLUORO-(5,6-DIHYDRO-2H-1,4-OXAZINE) IN THE PRESENCE OF FLUORIDE ANION

Citation
M. Nishida et al., POLYFLUOROALKYLATION AND POLYFLUOROALKOXYLATION OF PERFLUORO-(5,6-DIHYDRO-2H-1,4-OXAZINE) IN THE PRESENCE OF FLUORIDE ANION, Journal of fluorine chemistry, 91(1), 1998, pp. 1-3
Citations number
19
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
ISSN journal
00221139
Volume
91
Issue
1
Year of publication
1998
Pages
1 - 3
Database
ISI
SICI code
0022-1139(1998)91:1<1:PAPOP>2.0.ZU;2-S
Abstract
Polyfluorinated tertiary amines were synthesized by the reactions of p rimary alkyl triflates (RFCH2OSO2CF3, R-F = CF3, C2F5, CHF2) with the morpholide anion, preformed from perfluoro(5,6-dihydro-2H-1,4-oxazine) on treatment with potassium fluoride (in tetraglyme). In the case of (CF3)(2)CHOSO2CF3, polyfluoroalkoxylated oxazine was obtained by repla cement of the imidoyl fluorine. A similar imidoyl fluorine substitutio n reaction occurred in the treatment of perfluoro(5,6-dihydro-2H-1,4-o xazine) with polyfluoroalkylsiloxanes regardless of alkyl group variat ion. (C) 1998 Elsevier Science S.A. All rights reserved.