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γ-戊内酯作为氨基羰基化反应的替代生物质基介质的应用。

Application of γ-Valerolactone as an Alternative Biomass-Based Medium for Aminocarbonylation Reactions.

作者信息

Marosvölgyi-Haskó Diána, Lengyel Blanka, Tukacs József M, Kollár László, Mika László T

机构信息

Department of Inorganic Chemistry, University of Pécs, János Szentágothai Research Center, MTA-PTE Research Group for Selective Chemical Syntheses, Ifjúság u. 6., 7624, Pécs, Hungary.

János Szentágothai Research Center, MTA-PTE Research Group for Selective Chemical Syntheses, Ifjúság útja 20., 7624, Pécs, Hungary.

出版信息

Chempluschem. 2016 Nov;81(11):1224-1229. doi: 10.1002/cplu.201600389. Epub 2016 Sep 28.

DOI:10.1002/cplu.201600389
PMID:31964097
Abstract

γ-Valerolactone (GVL) was proposed as a renewable, nontoxic reaction medium with negligible vapor pressure for homogeneous Pd-catalyzed aminocarbonylation reactions. Iodobenzene as a model substrate and its 4-substituted derivatives were converted to the corresponding 2-ketocarboxamides with high conversions and chemoselectivities in γ-valerolactone. The effect of carbon monoxide pressure and reaction temperature on the conversion and selectivities were studied in the range 1-50 bar and 25-100 °C, respectively. The highest conversion and selectivity was achieved at 25 bar and 50 °C for iodobenzene in GVL for 24 h.

摘要

γ-戊内酯(GVL)被提议作为一种可再生、无毒且蒸气压可忽略不计的反应介质,用于均相钯催化的氨甲酰化反应。以碘苯作为模型底物及其4-取代衍生物,在γ-戊内酯中可高效转化为相应的2-酮羧酰胺,转化率和化学选择性都很高。分别研究了一氧化碳压力和反应温度在1-50 巴和25-100 °C范围内对转化率和选择性的影响。在GVL中,碘苯于25 巴和50 °C反应24小时时,可实现最高的转化率和选择性。

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