58700-10-0Relevant academic research and scientific papers
Reactions of 2,2-Dialkoxy Ketone Oximes with Chlorine and Bromine. Halogenation vs. Beckmann Fragmentation
Oxenrider, Bryce C.,Rogic, Milorad M.
, p. 2629 - 2633 (2007/10/02)
Reactions of 2,2-dialkoxycycloalkanone oximes with chlorine or bromine can be direct either to give 3-chloro- or 3-bromo-2,2-dialkoxycycloalkanone oximes or to undergo Beckmann fragmentation to give ω-(alkoxycarbonyl)alkanehydroximoyl halides.The resultin
Process for halogenating α,α-dialkoxyalkyl ketoximes
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, (2008/06/13)
A process is described for directly mono-brominating or mono-chlorinating α,α-dialkoxyalkyl or α,α-dialkoxycycloalkyl ketoximes in the β-position. Particularly described is the direct chlorination of 2,2-dimethoxycyclohexanone oxime to produce 3-chloro-2,
