Kinetics of 4-tert-butylphenol hydrogenation over rhodium

The kinetics of the liquid phase hydrogenation of 4‐tert‐butylphenol to form cis‐ and trans‐ 4‐tert‐butylcyclohexanol at 1.0–10.0 MPa and 40°C in isopropanol over a Rh catalyst has been studied. The kinetic behavior of this parallel system is described by a proposed reaction network. Keto‐enol tauto...

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Veröffentlicht in:Chemical engineering & technology 1997-02, Vol.20 (2), p.144-148
Hauptverfasser: Konuspaev, Sapar R., Zhanbekov, Khairulla N., Kul'Kova, Natalya V., Murzin, Dmitry Yu
Format: Artikel
Sprache:eng
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Zusammenfassung:The kinetics of the liquid phase hydrogenation of 4‐tert‐butylphenol to form cis‐ and trans‐ 4‐tert‐butylcyclohexanol at 1.0–10.0 MPa and 40°C in isopropanol over a Rh catalyst has been studied. The kinetic behavior of this parallel system is described by a proposed reaction network. Keto‐enol tautomeric transformation of adsorbed 4‐tert‐butyltetrahydrophenol and 4‐tert‐butylcyclohexanone is thought to be a key step, which governs the stereoselectivity of the overall complex reaction of alkylphenol hydrogenation.
ISSN:0930-7516
1521-4125
DOI:10.1002/ceat.270200212