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Synthesis of N-(3-rosin acyloxy-2-hydroxyl) Propyl-N,N Diethanolamine and Its Anti-fungal Activity

机译:合成N-(3-松香酰氧基-2-羟基)丙基-N,N二乙醇胺及其抗真菌活性

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Rosin was used as a raw material to prepare N-(3-rosin acyloxy-2-hydroxyl) propyl-N,N diethanolamine. First, rosin was modified with epoxy chloropropane. Then the modified rosin reacted with diethanolamine and N-(3-rosin acyloxy-2-hydroxyl) propyl-N, N diethanolamine was produced under the following conditions: modified rosin and diethanolamine mole ratio of 1:2, reaction temperature of 78°C, and reaction time of 2.5 h. The chemical structure of the product as a rosin amide derivative was identified by Fourier transform infrared spectroscopy (FTIR) and liquid chromatography-mass spectrometry (LC-MS) method. The anti-fungal activity of this rosinyl tertiary amine was determined in vitro against wood decay fungi, Trametes versicolor, Gloeophyllum trabeum and mould fungi, Aspergillus niger and Paecilomyces variot Bainier. The anti-fungal experiment results signified that N-(3-rosin acyloxy-2-hydroxyl) propyl-N,N diethanolamine was active to these fungi at a certain concentration.
机译:松香用作原料以制备N-(3-松香酰氧基-2-羟基)丙基-N,N二乙醇胺。首先,用环氧氯丙烷改性松香。然后在下列条件下制备与二乙醇胺和N-(3-松香酰氧基-2-羟基)反应的改性松香和N-(3-松香酰氧基-2-羟基羟基甲胺,产生1:2的松香和二乙醇胺摩尔比,反应温度为78°C ,反应时间为2.5小时。通过傅里叶变换红外光谱(FTIR)和液相色谱 - 质谱(LC-MS)方法鉴定产物作为松香酰胺衍生物的产品的化学结构。这种茂丙基叔胺的抗真菌活性在体外测定木腐烂真菌,Trametes Versicolor,Gloeophyllum Trabeum和霉菌真菌,曲霉尼日尔和Paecilomyces Variot Bainier。抗真菌实验结果表示N-(3-松香酰氧基-2-羟基)丙基-N,N二乙醇胺以一定浓度为这些真菌活性。

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