Aromatization of para-menthenic terpenes by aerobic oxidative dehydrogenation catalyzed by p-benzoquinone

• Published in: Applied catalysis. A, General General, 2008-12, Vol.351 (2), p.226-230
• Main Authors: Bueno, Aline C., Brandão, Bruno B.N.S., Gusevskaya, Elena V.
• Format: Article
• Language: English
• Subjects: Aromatization; Benzoquinone; Catalysis; Chemistry; Dioxygen; Exact sciences and technology; General and physical chemistry; Monoterpenes; Oxidative dehydrogenation; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry
• ISSN: 0926-860X; 1873-3875
• DOI: 10.1016/j.apcata.2008.09.023

The aerobic dehydrogenation of cheaply available para-menthenic terpenes, i.e., γ-terpinene, α-terpinene, limonene, and terpinolene, to commercially more valuable p-cymene has been developed. The reaction is catalyzed by p-benzoquinone and occurs in acetic acid solutions under relatively mild conditions (80–100 °C, 5–10 atm). In the presence of Cu(OAc) 2 as co-catalyst which accelerates the re-oxidation of p-hydroquinone to p-benzoquinone by molecular oxygen, the aerobic dehydrogenation can be performed even under atmospheric pressure. The reaction with γ-terpinene, the most reactive isomer, gives p-cymene in near quantitative yield and shows high turnover numbers (up to 1000). A solvent scope for this reaction can be extended to more friendly non-acidic alcoholic or amidic solvents. α-Terpinene also undergoes aromatization under similar conditions giving p-cymene in excellent yield (95%). On the other hand, the dehydrogenation of limonene and terpinolene, the substrates containing an exocyclic double bond, seems to be preceded by the double bond isomerization; so that these reactions require the presence of acid co-catalysts and give p-cymene in lower yields (ca. 60%). The aerobic dehydrogenation of cheaply available para-menthenic terpenes, i.e., γ-terpinene, α-terpinene, limonene, and terpinolene, to commercially more valuable p-cymene has been developed. The reaction is catalyzed by p-benzoquinone (BQ) and occurs under relatively mild conditions. The addition of Cu(OAc) 2, which catalyzes the re-oxidation of p-hydroquinone to BQ by molecular oxygen, significantly accelerates the reaction and allows to work under atmospheric pressure. ▪