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Difluoroamines, synthesis

Difluoroamine is one of the most suitable agents for the synthesis of organic difluoroamino and geminal bis(difluoroamino) derivatives of different classes of compounds (106, 109,121). [Pg.164]

Synthesis of the parent compound 150, cyclodiazomethane, from SchifT bases of formaldehyde and difluoroamine, also proceeds with dealkylation. ... [Pg.96]

Graham (1962) described a direct one-step synthesis of diazirine by the reaction of difluoroamine (HNF2) with er butyl- or octyl azomethine (H2C=N —R) in CCI4 solution in a vacuum system. A yield of 62<7o was reported without any further information on mechanistic details. It seems that dealkylation and defluorination take place in the transient l-alkyl-2-fluoro-diaziridine (5.62, 5-15). [Pg.175]


See other pages where Difluoroamines, synthesis is mentioned: [Pg.325]    [Pg.647]    [Pg.180]    [Pg.306]    [Pg.80]    [Pg.95]   
See also in sourсe #XX -- [ Pg.632 , Pg.634 , Pg.647 ]




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Difluoroamine

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