Formation of 1,1-dihalogeno-4-methylpenta-1,4-dienes by reactionof isobutene with trihalogenoethylenes
Abstract
Isobutene reacts with trihalogenoethylenes in the gas phase at ca. 500° to give 1,1-dihalogeno-4-methylpenta-1,4-dienes which are precursors of photostable pyrethroid insecticides. The reaction appears suited to large scale continuous operation. The results are interpreted in terms of a free-radical chain mechanism.