摘要
以芳醛、2-萘胺和Meldrum酸为原料,以水为溶剂,在回流条件下以三乙基苄基氯化铵为催化剂通过三组分一锅反应,合成了一系列的1-芳基苯并[f]喹啉衍生物.该方法具有反应条件温和、产率较高(79%~87%)、环境友好等优点.产物的结构通过熔点,IR,1H NMR和元素分析表征.
A series of 1-aryl-1,2-dihydrobenzo[f]quinolin-3(4H)-one derivatives were synthesized by a three-component one-pot reaction of benzaldehyde, naphthalene-2-amine and meldrum's acid at refluxing temperature catalyzed by triethylbenzylammonium chloride in water. This method has the advantages of milder reaction conditions, good yields (79%-87%) and environmental benignity. The structures of the products were characterized by melting points, IR, ^1H NMR spectra and elemental analysis.
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2008年第5期881-884,共4页
Chinese Journal of Organic Chemistry
基金
江苏省高校自然科学基金(No.04KJB150139)
徐州师范大学校自然科学基金(No.06XLA10)资助项目
关键词
苯并[f]喹啉
水
三乙基苄基氯化铵
合成
benzo[f]quinoline
water
triethylbenzylammonium chloride
synthesis