Photochemistry of Hantzsch 1,4-dihydropyridines and pyridines

Abstract

The photochemistry of some Hantzsch 4-phenyl-1,4-dihydropyridines bearing a substituent on the phenyl ring (the three isomeric chloro derivatives and the 4′-nitro derivative) has been studied. All of these compounds underwent inefficient aromatization to the corresponding pyridines (quantum yield <10 −4 at 366 nm, <10 −2 at 254 nm). This process is scarcely affected by molecular oxygen and is initiated by proton transfer (from C 4–H), probably to the solvent, from the excited singlet. In turn, the thus formed pyridines were photoreactive with comparable or higher efficiency. Thus, the 4-(3′-chlorophenyl) and 4-(4′-chlorophenyl) Hantzsch pyridines underwent positional rearrangement to form two isomers each. The reaction occurs via Dewar benzene--prismane path. In the case of the minor isomer a further 1,3-shift take place at the Dewar benzene level. The 4-(2′-chlorophenyl) derivative underwent C–Cl bond homolysis, which led to cyclization of the phenyl group onto one of the ester groups forming a pyrane ring.