1202752-67-7Relevant articles and documents
Regioselective Synthesis of Polyfluoroalkyl Substituted 6,7-Dihydrobenzisoxazolones
Khlebnicova, Tatyana S.,Piven', Yurii A.,Isakova, Veronica G.,Baranovsky, Alexander V.,Lakhvich, Fedor A.,Sorochinsky, Alexander E.,Gerus, Igor I.
, p. 1791 - 1797 (2018/07/24)
Regioselective methods for synthesis of hitherto unreported both 6,7-dihydro-1,2-benzisoxazol-4(5H)-ones and 6,7-dihydro-2,1-benzisoxazol-4(5H)-ones with perfluoroalkyl or halogenodifluoromethyl substituents have been developed. 3-Polyfluoroalkyl-6,7-dihydro-1,2-benzisoxazol-4(5H)-ones were prepared by the cyclocondensation of 2-polyfluoroalkanoylcyclohexane-1,3-diones with hydroxylamine. The regioisomeric 3-polyfluoroalkyl-6,7-dihydro-2,1-benzisoxazol-4(5H)-ones were synthesized by the transformation of 2-polyfluoroalkanoylcyclohexane-1,3-diones into their vinylogous chlorides, followed by the interaction of obtained crude 3-chloro-2-polyfluoroalkanoyl-2-cyclohexen-1-ones with sodium azide in dimethylformamide.
Reaction of 2-perfluoroalkanoylcyclohexane-1,3-diones and 3-chloro-2-perfluoroalkanoylcyclohex-2-ene-1-ones with amines
Khlebnikova,Isakova,Lakhvich
experimental part, p. 993 - 1001 (2011/02/26)
Reactions of 2-perfluoroalkanoylcyclohexane-1,3-diones with primary and secondary amines involved acid cleavage of the substrate with formation of the corresponding 3-aminocyclohex-2-en-1-ones. Vinylogous nucleophilic substitution in 3-chloro-2-perfluoroa