Refluxing 4-hydroxypyridine and alpha,alpha'-dibromo-o-xylene in an et
hanolic sodium ethoxide solution affords alpha,alpha'-di(4-pyridon-1-y
l)-o-xylene (1) which undergoes a novel [2+2] photocycloaddition react
ion in 3:7 ethanol-ether giving .20(5,15).0(6,16)]hexadeca-2,8-diene-4
,7-dione(2). The structure of 2 was determined by x-ray crystallograph
ic analysis.