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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Environmentally friendly, heterogeneous acid and base catalysis for the methylation of catechol: Chances for the control of chemo-selectivity
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Environmentally friendly, heterogeneous acid and base catalysis for the methylation of catechol: Chances for the control of chemo-selectivity

机译:环保的异质酸和碱催化儿茶酚的甲基化:控制化学选择性的机会

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摘要

The properties of catalysts with (i) Bronsted-type acidity (H-mordenite and Al/P mixed oxide), (ii) Lewis-type acidity (At trifluoride) or (iii) basic characteristics (Mg/Fe mixed oxide) were investigated in the gas-phase methylation of catechol. When methanol was used as the methylating agent, H-mordenite and AlF3 gave high selectivities to guaiacol (the product of O-methylation) under mild reaction conditions, that is at very low catechol conversions. An increase in temperature led to the transformation of guaiacol to phenol and cresols, and to considerable catalyst deactivation. The basic catalyst Mg/Fe/O also favored an extensive degradation of guaiacol to phenol. On the mildly acidic catalyst Al/P mixed oxide a stable catalytic perfon-nance and a high selectivity to guaiacol at 40% catechol conversion were obtained. When methylformate, a more reactive methylating agent, was used with AlF3 and Mg/Fe mixed oxide as catalysts, higher catechol conversions and slower deactivation rates could be achieved under mild reaction conditions, with a low extent of guaiacol degradation. However, methylformate rapidly decomposed when temperatures above 350 degrees C were used. Finally, tests were made by reacting catechol and diethoxymethane with acid catalysts, with the aim of synthesizing methylenedioxybenzene. The latter product was obtained with high selectivity, but with very low yield, due to both catalyst deactivation and decomposition of diethoxymethane. (c) 2006 Elsevier B.V. All rights reserved.
机译:研究了(i)布朗斯特型酸度(H-丝光沸石和Al / P混合氧化物),(ii)路易斯型酸度(三氟化物时)或(iii)基本特性(Mg / Fe混合氧化物)的催化剂的性能在邻苯二酚的气相甲基化中。当甲醇用作甲基化剂时,H-丝光沸石和AlF3在温和的反应条件下,即邻苯二酚的转化率非常低时,对愈创木酚(O-甲基化的产物)具有很高的选择性。温度升高导致愈创木酚转化为苯酚和甲酚,并使催化剂大量失活。碱性催化剂Mg / Fe / O还有助于将愈创木酚广泛降解为苯酚。在弱酸性催化剂Al / P混合氧化物上,在40%的邻苯二酚转化率下获得了稳定的催化性能和对愈创木酚的高选择性。当将具有更高反应活性的甲基化剂甲酸酯与AlF3和Mg / Fe混合氧化物一起用作催化剂时,在温和的反应条件下,可以实现较高的儿茶酚转化率和较低的失活速率,且愈创木酚的降解程度较低。但是,当使用温度高于350摄氏度时,甲酸甲酯会迅速分解。最后,通过合成邻苯二酚和二乙氧基甲烷与酸催化剂进行测试,以合成亚甲基二氧基苯。由于催化剂失活和二乙氧基甲烷的分解,以高选择性但以非常低的收率获得了后一种产物。 (c)2006 Elsevier B.V.保留所有权利。

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