The Prilezhaev reaction, also known as the Prileschajew reaction or Prilezhaev epoxidation, is the chemical reaction of an alkene with a peroxy acid to form epoxides. It is named after Nikolai Prilezhaev, who first reported this reaction in 1909. A widely used peroxy acid for this reaction is meta-chloroperoxybenzoic acid, due to its stability and good solubility in most organic solvents. An illustrative example is the epoxidation of trans-2-butene with m-CPBA to give trans-2,3-epoxybutane: The reaction is highly stereospecific in the sense that the double bond stereochemistry is generally transferred to the relative configuration of the epoxide with essentially perfectfidelity, so that a trans-olefin leads to the stereoselective formation of the trans-2,3-substituted epoxide only, as illustrated by the example above, while a cis-olefin would only give the cis-epoxide. This stereochemical outcome is a consequence of the accepted mechanism, discussed below.
Reaction mechanism
The reaction proceeds through what is commonly known as the "butterfly mechanism", first proposed by Bartlett, wherein the peracid is intramolecularly hydrogen-bonded at the transition state. Although there are frontier orbitalinteractions in both directions, the peracid is generally viewed as the electrophile and the alkene as the nucleophile. In support of this notion, more electron-rich alkenes undergo epoxidation at a faster rate. For example, the relative rates of epoxidation increases upon methyl substitution of the alkene : ethylene, propene, cis-2-butene, 2-methyl-2-butene, 2,3-dimethyl-2-butene. The reaction is believed to be concerted, with a transition state that is synchronous or nearly so. The "butterfly mechanism" takes place via a transition state geometry in which the plane of the peracid bisects that of the alkene, with the O–O bond aligned perpendicular to it. This conformation allows the key frontier orbital interactions to occur. The primary interaction of the occupied πC=C orbital and the low-lying unoccupied σ*O-O orbital. This interaction accounts for the observed overall nucleophilic character and electrophilic character of the alkene and peracid, respectively. There is also a secondary interaction between a lone pair orbital perpendicular to the plane of the peracid, nO and the unoccupied π*C=C orbital. Using the approach of Anslyn and Dougherty, the mechanism can be represented as follows: There is a very large dependence of the reaction rate on the choice of solvent.
