FURAN RING FORMATION IN OH-INITIATED PHOTOOXIDATION OF 1,3-BUTADIENE AND cis-1,3-PENTADIENE.

Article abstract of DOI:10.1246/bcsj.57.960

Reactions of hydroxyl radicals with 1,3-butadiene and cis-1,3-pentadiene in the presence of oxygen were studied in the gas phase. Two OH radical sources were employed; photolysis of H//2O//2 at 254 nm and photolysis of methyl nitrite at 360 nm. In the reaction system for 1,3-butadiene, furan was detected besides acrylaldehyde and in the cis-1,3-pentadiene system, 2-methylfuran was detected besides acetaldehyde, acrylaldehyde, and croton-aldehyde by gas chromatographic analysis. Approximate yields of furan and 2-methylfuran were 5. 3-6. 7% and 6. 7-8. 4%, respectively, which were sensitive to the conditioning of the surface of reactor but insensitive to hydroxyl radical sources, the surface material of reaction vessel or the surface to volume ratio reactors. The yields of aldehydes were also measured.