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首页> 外文期刊>Ultrasonics sonochemistry >Benign methodology and improved synthesis of 5-(2-chloroquinolin-3-yl)-3- phenyl-4,5-dihydroisoxazoline using acetic acid aqueous solution under ultrasound irradiation
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Benign methodology and improved synthesis of 5-(2-chloroquinolin-3-yl)-3- phenyl-4,5-dihydroisoxazoline using acetic acid aqueous solution under ultrasound irradiation

机译:超声辐射下乙酸水溶液的良性方法和5-(2-氯喹啉-3-基)-3-苯基-4,5-二氢异恶唑啉的改进合成

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摘要

In the present paper, we have executed the synthesis of substituted 5-(2-chloroquinolin-3-yl)-3-phenyl-4,5-dihydroisoxazolines via the reactions of substituted 3-(2-chloroquinolin-3-yl)-1-phenylprop-2-en-1-ones with hydroxylamine hydrochloride and sodium acetate in aqueous acetic acid solution in 72-90% yields at room temperature under ultrasound irradiation. This method provides several advantages such as operational simplicity, higher yield, safety and environment friendly protocol. The resulting substituted isoxazolines were characterized on the basis of 1H NMR, 13C NMR, IR, elemental analysis, and mass spectral data.
机译:在本文中,我们通过取代的3-(2-氯喹啉-3-基)-的反应进行了取代的5-(2-氯喹啉-3-基)-3-苯基-4,5-二氢异恶唑啉的合成乙酸水溶液中的1-苯基丙-2-烯-1-酮与盐酸羟胺和乙酸钠的溶液在室温下超声辐照下的收率为72-90%。这种方法具有许多优点,例如操作简便,产率更高,安全性和环境友好协议。根据1 H NMR,13 C NMR,IR,元素分析和质谱数据表征所得的取代的异恶唑啉。

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