Yq. Song et al., THE PHOTOLYSES OF 2,6-DIFLUOROHALOBENZENES AND 2,4-DIFLUOROHALOBENZENES, Bulletin of the Chemical Society of Japan, 70(8), 1997, pp. 1875-1878
Photolyses of 2,6- and 2,4-difluorobromobenzenes in acetonitrile gave
isomerized and brominated products in addition to 1,3-difluorobenzene
produced by the dehalogenation. The reactions were compared with simil
ar reactions of the corresponding chloro-and iodoarenes. In general, p
hotolytic cleavage of the C-X bond of 2,6-difluorohalo(X)benzene was s
hown to proceed more easily than the corresponding 2,4-diffuorohalo co
mpound.