Abstract
A highly efficient synthesis of cyclic carbonates from olefins and CO2 has been achieved by the use of a molybdenyl acetylacetonate (MoO2(acac)2)–quaternary ammonium salt catalytic system with tert-butyl hydroperoxide as an oxidant through a one-pot multistep process. This simple and cheap method can be applied to various olefins, such as 1-octene, 1-hexene, allyl chloride, cyclohexene and styrene, affording the highest yields in comparison with the data reported previously except for styrene. A plausible mechanism is proposed based on the results.
Original language | English |
---|---|
Pages (from-to) | 2518-2524 |
Number of pages | 7 |
Journal | Green Chemistry |
Volume | 13 |
Issue number | 9 |
DOIs | |
Publication status | Published - 30 Aug 2011 |