摘要
芳并吡喃-4-酮骨架存在于许多天然及合成的生物活性物质中,因此发展其高效合成方法极具实用价值.本工作以氯化铁为催化剂催化3-甲基巴豆酸萘酯转化生成一系列2,3-二氢苯并色原酮,由原料通过发生Fries重排/氢烷氧化串联反应生成目标化合物.该方法所用催化剂价廉易得,转化效率较高,为合成芳并吡喃-4-酮类化合物提供了一种经济,实用和高效的新方法.
Aromatic-fused pyran-4-one skeleton exists in many natural and synthetic biologically active materials. An efficient method for the transformation of naphthyl 3-methylcrotonate to 2,3-dihydro-benzo[f]chromen-1-one catalyzed by ferric chloride is described, which provides a practical process to afford this type of biologically important compounds in good yields using commercially available and inexpensive catalyst. A two-step mechanism involving Fries rearrangement and intramolecular hydroalkoxylation is proposed.
作者
丁晓友
徐凡
Ding Xiaoyou;Xu Fan(College of Chemistry,Chemical Engineering and Materials Science,Sooehow University,Suzhou 215123)
出处
《有机化学》
SCIE
CAS
CSCD
北大核心
2018年第12期3345-3350,共6页
Chinese Journal of Organic Chemistry
基金
国家自然科学基金(No.21272168)资助项目~~