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Chemo- and Regioselective Synthesis of Arylated gamma-Valerolactones from Bio-based Levulinic Acid with Aromatics Using H-beta Zeolite Catalyst

机译:使用H-β沸石催化剂将来自生物基乙酰丙酸的芳酸化γ-缬氨酸的细化学和区域选择性

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摘要

Catalytic coupling of biomass-based molecules to value-added chemical intermediates is an interesting area in biomass research. Arylated gamma-valerolactones (Agvls), promising pharmaceutical intermediates that have significant biological activity, are primarily synthesized currently through petro-route. In this paper, we report successful biomass-based synthesis of Agvls using levulinic acid (LA) and oxygen or sulphur- substituted aromatics over H-beta zeolite as catalyst under solvent-free conditions. Under optimized condition, LA and anisole render 90% conversion of former with 82% yield of para-substituted gamma-lactone. C-C bond formation followed by intra-molecular esterification is witnessed in the course of the reaction, which is highly chemo- and regioselective. Though catalyst deactivated while reuse due to deposition of organic carbon moieties as deduced from several physicochemical techniques, it could be regenerated by simple calcination.
机译:生物质基分子对增值化学中间体的催化偶联是生物质研究中的一个有趣区域。 芳族γ-戊内酯(AGV1),具有显着生物活性的有明显的生物活性的药物中间体主要通过石油途径合成。 在本文中,我们在无溶剂条件下报告在H-Beta沸石上使用紫水酸(La)和氧气或硫取代的芳烃在H-Beta沸石上的成功合成AGV1。 在优化的条件下,La和α10%含有82%的对丙烷 - 内酯的成品90%。 在反应过程中,在反应过程中得到了C-C键形成,然后在反应过程中得到了高度化学和区域选择性。 虽然催化剂由于从几种物理化学技术推导出的有机碳部分的沉积而被停用,但是通过简单的煅烧可以再生。

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