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作 者:张峰[1] 孙继奎[1] 李亚卓[1] 高大维[1] 张玉敏[1] 赵天琦[1] 陈晓东[2]
机构地区:[1]吉林大学化学学院,吉林长春130012 [2]吉林大学测试科学实验中心,吉林长春130023
出 处:《精细化工》2007年第4期409-412,共4页Fine Chemicals
摘 要:分别以吡啶和三乙胺为催化剂,在传统加热和微波辐射两种条件下对5种目标产物进行了合成,其中目标产物Ⅱ、Ⅳ和Ⅴ经科技查新证实均属国内外文献未公开报道的新型化合物,其新颖性已为教育部科技查新工作站(吉林大学查新检索咨询中心)的200604311212号《科技查新报告》所证实。以吡啶为催化剂,目标产物产率由传统加热下的61.6%提高到微波辐射下的81.6%,反应时间缩短为传统的1/100;以三乙胺为催化剂,目标产物产率由传统加热下的75.2%提高到微波辐射下的94.4%,反应时间缩短为传统的1/15。通过元素分析、MS谱、1HNMR谱对所合成的目标产物分别进行了全面的表征,证实了其分子结构。并对5种目标产物进行了紫外测试,得出其最大吸收峰在315 nm左右。实验结果表明:当糠偶姻的用量为20 mmol时,最适宜反应条件为:n(糠偶姻)∶n(酰氯)=1∶2.2,有机碱三乙胺的用量为25 mL,微波工作功率为240 W,辐射时间10 min,产率94%以上。The target products were synthesized in the presence of pyridine and triethylamine as catalysts under traditional calefaction and microwave irradiation. With pyridine as catalyst, the yield was raised from 61.6% (under traditional calefaction) to 81.6% (under microwave irradiation),and the reaction time was decreased to 1/100 times. With triethylamine as catalyst, the yields raised from 75.2% ( under traditional calefaction) to 94.4% ( under microwave irradiation), and the reaction time was decreased to 1/15 times. By characterization with elementary analysis, MS and ^1HNMR, the structural formula of 5 target products were distinctively demonstrated. Their max. UV absorbance were near 315 nm. The experimental results show the best synthesis conditions :furoin 20 retool, n (furoin): n( acid chloride) = 1:2.2, triethylanine 25 mL, power of microwave 240 W and radiation time 10 min. Yields of the products were over 94%.
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