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学術論文

Synthesis of Butyl Levulinate Based on α-Angelica Lactone in the Presence of Easily Separable Heteropoly Acid Catalysts

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Al Shaal,  Mohammad Ghith
Research Department Schüth, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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Palkovits,  Regina
Chair of Heterogeneous Catalysis and Chemical Technology, RWTH Aachen University, Aachen, Germany;
Research Group Palkovits, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

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引用

Yi, X., Al Shaal, M. G., Ciptonugroho, W., Delidovich, I., Wang, X., & Palkovits, R. (2017). Synthesis of Butyl Levulinate Based on α-Angelica Lactone in the Presence of Easily Separable Heteropoly Acid Catalysts. ChemSusChem. doi:10.1002/cssc.201601882.


要旨
A series of choline (Ch)-exchanged heteropoly acids (HOCH2CH2N(CH3)3)xH(6−x)P2W18O62 [abbreviated as ChxH(6−x)P2W18O62, x=1–6] was synthesized and used as catalysts for the reaction of α-angelica lactone (alpha-AL) with n-butanol to form butyl levulinate (BL). The solubility of ChxH(6−x)P2W18O62, in the reaction mixture was temperature dependent: The catalysts were soluble under the reaction conditions and precipitated upon cooling of the reaction mixture. This facilitated recovery of the catalysts from the liquid phase. Importantly, an increase of the Ch content caused a decrease of the catalyst solubility. Catalytic activity of ChxH(6−x)P2W18O62, for the reaction with n-butanol appeared to be in good agreement with the concentration of Brønsted-acidic sites. The results suggest that the reaction proceeded through formation of pseudo-butyl levulinate as intermediate. ChxH(6−x)P2W18O62, exhibited the best balance between catalytic activity and temperature-dependent solubility. The yield of BL reached 79.4 % at full conversion of alpha-AL at a moderate temperature of 75 °C in an open system. ChxH(6−x)P2W18O62, could be successfully reused five times without significant loss of activity.