Abstract
The epoxidation of C5 to C8 olefins with hydrogen peroxide (30%) was studied on molybdenum oxide-Bu3SnCl-charcoal in isopropyl alcohol at 50°C. The yields were remarkably increased by using chemically pretreated charcoals as supports. As modifiers of charcoal, butylating or trimethylsilylating agents gave good results. Cycloolefins of C5 to C8 and an inner olefin, 2-octene, selectively gave epoxides in 90 to 70% yields compared with yields of 60 to 40% on the catalyst prepared from raw charcoal. The increase in yield was attributed to the prevention of the decomposition of hydrogen peroxide.