Vanadium-based highly active and selective catalysts for oxidative dehydrogenation of ethyl lactate to ethyl pyruvate
[Display omitted] •Vanadium based catalysts for efficient oxidative dehydrogenation of ethyl lactate to ethyl pyruvate under mild conditions.•Aqueous TBHP as an efficient oxidant with homogenous and heterogeneous vanadium catalysts.•Homogeneous catalysts showed very high ethyl lactate conversion and...
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Published in: | Applied catalysis. A, General Vol. 587; p. 117246 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Elsevier B.V
25-10-2019
Elsevier |
Series: | Applied Catalysis A : General |
Subjects: | |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Vanadium based catalysts for efficient oxidative dehydrogenation of ethyl lactate to ethyl pyruvate under mild conditions.•Aqueous TBHP as an efficient oxidant with homogenous and heterogeneous vanadium catalysts.•Homogeneous catalysts showed very high ethyl lactate conversion and 100% ethyl pyruvate selectivity at room temperature.•V2O5 serves as an efficient catalyst with almost 98% conversion and 100% ethyl pyruvate selectivity at 80 °C.•V2O5 serves as recyclable heterogeneous catalyst without compromising the activity.
Pyruvates are important intermediates for various bioactive and pharmaceutical molecules. Synthesis of pyruvates is challenging due to low selectivity, as the pyruvates are prone to polymerisation. In the present work, oxidative dehydrogenation of ethyl lactate to ethyl pyruvate was carried out under very mild conditions using vanadium-based homogeneous and heterogeneous catalysts in the presence of aqueous t-butyl hydroperoxide as an oxidant. Homogenous vanadium-based catalyst, VO(acac)2 in acetonitrile solvent, gave excellent conversion (upto 83%) with 100% selectivity to ethyl pyruvate at room temperature. However, the heterogeneous catalyst, V2O5 exhibited very high activity for oxidative dehydrogenation of ethyl lactate only at higher temperature (80 °C). At higher temperature, significant TBHP decomposition was observed if all TBHP was added in one lot. In case of ethyl lactate dehydrogenation using V2O5 catalyst at 80 °C with two equivalents TBHP, 60% ethyl lactate conversion with 100% TBHP conversions were observed after 5 h when all TBHP was added initially in the reaction mixture. However, the ethyl lactate conversion at 80 °C, after 5 h increased to 72% when the same amount of TBHP was added batch wise over a period of 4 h, indicating improved conversion of TBHP to ethyl pyruvate. The heterogeneous catalyst, V2O5 exhibited up to 98% conversion with 100% ethyl pyruvate selectivity at 80 °C after 10 h with 3 equivalent TBHP added batch wise. The homogeneous catalyst could not be reused while V2O5 could be successfully recycled five times without catalytic performances loss. Oxidation proceeds by radical mechanism, as proved by experiment with radical scavenger. |
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ISSN: | 0926-860X 1873-3875 |
DOI: | 10.1016/j.apcata.2019.117246 |