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Keggin型杂多酸催化合成1-乙酰胺基苯甲基-2-萘酚 被引量:7

Synthesis of N-[Phenyl-(2-Hydroxy-Napthalen-1-yl)-Methyl]-Acetamide Catalyzed by Keggin-Structured Heteropolyacids
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摘要 以2-萘酚、苯甲醛和乙酰胺为原料、Keggin型杂多酸及磷钨酸盐为催化剂,采用无溶剂一步法经多组分缩合反应合成了1-乙酰胺基苯甲基-2-萘酚(AAN);比较了一系列Keggin型杂多酸及磷钨酸盐的催化效果。实验结果表明,磷钨酸的催化活性最高。同时考察了在磷钨酸催化剂作用下,催化剂用量、反应温度、原料配比和反应时间对AAN收率的影响,确定了适宜的反应条件:磷钨酸用量为反应物总质量的8.0%、n(苯甲醛)∶n(乙酰胺)∶n(2-萘酚)=1.15∶1.00∶1.00、反应温度120℃、反应时间40min;在此条件下,AAN的收率达到100.0%。该工艺具有催化剂用量较少、AAN收率高、反应速率快、后处理简单及产物色泽好等优点。 N- [ phenyl- ( 2-hydroxy-napthalen -1 -yl ) -methyl] -acetamide (AAN) was synthesized by multi-component one-step condensation of 2-naphthol, benzaldehyde and acetamide with 12- tungstophosphoric acid as catalyst without solvent. A series of Keggin-structured heteropoly compounds, namely 12-tungstophosphoric acid and its aluminum, ammonium, potassium and cesium salts, 12-silicotungstic acid, 12-phosphomolybdic acid, 10-molybdo-2-vanadophosphoric acid and 9- molybdo-3-vanadophosphoric acid, were considered as catalysts for synthesis of AAN. 12- Tungstophosphoric acid showed the best catalytic activity for the reaction. Under optimal reaction conditions: catalyst mass fraction in reaction system 8. 0%, reaction temperature 120℃, n(benzaldehyde) : n(acetamide) : n(2-naphthol) 1.15 : 1.00 : 1.00 and reaction time 40 min, yield to AAN reached 100.0%. The process features excellent yield to AAN, short reaction time, low catalyst consumption and simple operation.
出处 《石油化工》 CAS CSCD 北大核心 2009年第3期299-303,共5页 Petrochemical Technology
基金 国家自然科学基金项目(20476046 20776069)
关键词 2-萘酚 苯甲醛 乙酰胺 1-乙酰胺基苯甲基-2-萘酚 磷钨酸 杂多酸 催化 多组分缩合反应 2-naphthol benzaldehyde acetamide N- [phenyl- ( 2-hydroxy-napthalen-l-yl ) - methyl] -acetamide 12-tungstophosphoric acid heteropolyacid catalysis multi-component condensation reaction
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参考文献15

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