This isn't really kitchen chem compatable, but I'm wondering about flourination of desirable compounds, yeilding things like DO(triflouromethyl),
2C-(triflouromethyl), and 3,5 dimethoxy 4- triflouromethyl phenethylamine and phenisopropyl amine.
for 2C-TF would one could a vilsmeyer rxn be performed on 2,5 dimethoxy 1 TFM benzene? Or would the TFM group be too electron withdrawing. Or perhaps start with 2 TFM hydroquinone in a basic solution, and do an ortho formylation, then methylate. I've only seen two halogenation reactions, replacement of halogen by KF/ 18- Crown-6 ether, and replacement of a diazonium salt by flouboric acid. Neither of those seem very applicable. Any help or even interest in this topic?
try
www.flourosolutions.com and ask the from a business account.
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