A new chemical process is proposed for the oxidation of cyclic olefins, such as cyclooctene and cyclododecene, to cyclic ketones in the presence of hydrogen peroxide and a catalytic system based on tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)(4)). The kinetic equation of the cyclooctene oxidation can be expressed by r(olefin) = k[olefin]([catalyst] - k'[H+](1.7)). Note that the reaction rate increases linearly with catalyst and olefin concentration and depends on the H+ concentration. The catalyst retains its activity when bound to a polymer. This allows catalyst recycling and better control of the reaction medium. Unlike most common processes for cyclic ketone production, the proposed novel method occurs in a single step and does not require any cocatalyst.
Kinetic study of cycloolefin oxidation with a Pd(0) complex / DE FILIPPIS, Paolo; Giavarini, Carlo; Rossella, Silla. - In: INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH. - ISSN 0888-5885. - STAMPA. - 37:5(1998), pp. 1769-1773. [10.1021/ie970671e]
Kinetic study of cycloolefin oxidation with a Pd(0) complex
DE FILIPPIS, Paolo;GIAVARINI, Carlo;
1998
Abstract
A new chemical process is proposed for the oxidation of cyclic olefins, such as cyclooctene and cyclododecene, to cyclic ketones in the presence of hydrogen peroxide and a catalytic system based on tetrakis(triphenylphosphine)palladium(0) (Pd(PPh3)(4)). The kinetic equation of the cyclooctene oxidation can be expressed by r(olefin) = k[olefin]([catalyst] - k'[H+](1.7)). Note that the reaction rate increases linearly with catalyst and olefin concentration and depends on the H+ concentration. The catalyst retains its activity when bound to a polymer. This allows catalyst recycling and better control of the reaction medium. Unlike most common processes for cyclic ketone production, the proposed novel method occurs in a single step and does not require any cocatalyst.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.