38727-31-0Relevant academic research and scientific papers
Reactions of polyfluoroarenes with hexamethyldisilazane and with 1,1,1-trimethyl-N,N-bis(trimethylsilyl)stannaneamine in the presence of caesium fluoride
Miller, Alexey O.,Furin, Georgii G.
, p. 169 - 172 (2007/10/03)
Hexamethyldisilazane and 1,1,1-trimethyl-N,N-bis(trimethylsilyl)stannaneamine aminate pentafluoropyridine, octafluorotoluene, pentafluorobenzonitrile, pentafluoronitrobenzene and pentafluorobenzene sulphonyl fluoride in the presence of caesium fluoride with formation of the corresponding perfluorinated aryl amines (ArNH2), diarylamines (Ar2NH) and triarylamines (Ar3N) (where the amine functions are in positions 4 relative to the arene substituent). - Keywords: Polyfluoroarenes; Hexamethyldisilazane; Caesium fluoride; Silylated amines
REACTION OF AROMATIC COMPOUNDS WITH NUCLEOPHILIC REAGENTS IN LIQUID AMMONIA. X. AMINATION OF POLYFLUORINATED AROMATIC COMPOUNDS CONTAINING ELECTRON-WITHDRAWING SUBSTITUENTS
Selivanova, G. A.,Chuikova, T. V.,Shtark, A. A.,Shteingarts, V. D.
, p. 2267 - 2272 (2007/10/02)
It was shown for the case of 2,4-difluoro-, 2,4,6-trifluoro-, and pentafluoronitrobenzenes that both liquid ammonia and sodium amide in liquid ammonia are effective reagents for aminodefluorination with respect to the fluorine derivatives of nitrobenzene.The observed tendency for the ortho-orientation with respect to the nitro group to change to para-orientation with increase in the number of fluorine atoms is more clearly defined for sodium amide than for liquid ammonia as nucleophile on account, clearly, of the stabilization of the transition state of ortho-substitution in the latter case by an intramolcular hydrogen bond.
