Abstract

The reaction of 10-methylacridinium cation (MA +) with isopropanol in the parent alcohol medium under dark, oxygen-free, and refluxing conditions gave hydride transfer product 10-methyl-9,10-dihydroacridine (MAH). The kinetics of the alcoholic oxidation reaction, including the kinetic isotope effect and the kinetic temperature effect, were determined. Hydride transfer is involved in the rate-determining step.

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