A Novel Two-Step Conversion of Lignin-Derived Phenol to Benzene Through Hydrogenation and Dehydrogenation
Related Experiment Video
Updated: Jul 12, 2026

Efficient Synthesis of Polyfunctionalized Benzenes in Water via Persulfate-promoted Benzannulation of α,β-Unsaturated Compounds and Alkynes
Published on: December 16, 2019
Riyang Shu1, Guangming Liang1, Hongyun You1
1Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, School of Materials and Energy, Guangdong University of Technology, Guangzhou, China.
Abstract:
Arenes possess high energy density and outstanding combustion performance, making them key components of aviation fuels. However, the conversion of lignin-derived phenolic compounds to arenes typically requires high temperatures (above 300°C), which not only alters the catalyst structure and promotes side reactions but also increases energy consumption and potential safety risks. In this study, a green and environmentally friendly two-step method for the low-temperature conversion of phenol to benzene was proposed, achieving controllable product selectivity at low temperatures. The hydrogenation of phenol occurred efficiently at room temperature and achieved 100% conversion of cyclohexanol. Then, the dehydration and dehydrogenation of cyclohexanol was performed at a low temperature of 200°C, resulting in 90.1% selectivity of benzene. In addition, the catalyst showed good cycling stability, with the benzene selectivity remaining at 84.6% after four reaction cycles. Based on the effect of reaction time on product distribution, a proposed reaction pathway for cyclohexanol to benzene was discussed. Moreover, the comparison between this two-step method and previously reported one-step methods for phenol to benzene was carried out, highlighting the superiority of this work.
Related Concept Videos
Benzene to Phenol via Cumene: Hock Process
Hydrolysis of Chlorobenzene to Phenol: Dow Process
Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation
Electrophilic Aromatic Substitution: Sulfonation of Benzene
Benzene to 1,4-Cyclohexadiene: Birch Reduction Mechanism
Reactions at the Benzylic Position: Oxidation and Reduction

