Abstract
Alkoxyl radicals, generated by nitrite photolysis, react with trifluoronitrosomethane to yield NN′-dialkoxy-NN′-bis-(trifluoromethyl)hydrazines. An 18O-labelling experiment indicated complete retention of the alkoxy-oxygen atom. When the products are heated with thioglycolic acid, cracking leads to the hydroxylamines, RO·NH·CF3. For the case where R is 1-adamantyl, further stepwise conversion into O-(1-adamantyl)hydroxylamine has been achieved.
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