Pyridylketenes. Structure reactivity effects in nucleophilic and radical addition

2-, 3-, and 4-Pyridylketenes have been generated in CH CN by photochemical Wolff rearrangements and identified by their ketenyl absorption in the infrared at 2127, 2125, and 2128 cm , respectively. Reaction of these pyridylketenes with -BuNH results in the formation of intermediate amide enols from the 3- and 4-pyridylketenes, which are then converted to the corresponding pyridylacetamides. However , 2-pyridylketene forms a long-lived 1,2-dihydropyridine intermediate stabilized by an intramolecular hydrogen bond, and this is converted to the 2-pyridylacetamide with a rate constant 10 less than those for the conversion of the amide enols from the 3- and 4-pyridylketenes to amides. Hydration of the pyridylketenes results in the formation of an acid enol intermediate in the case of the 3-isomer, while the 2- and 4-isomers form longer-lived dihydropyridines. The pyridylketenes react with the stable free radical tetramethylpiperidinyloxyl (TEMPO,TO) forming 1,2-diaddition products ArCH(OT)CO T.