有机化学 ›› 2018, Vol. 38 ›› Issue (12): 3345-3350.DOI: 10.6023/cjoc201806007 上一篇    下一篇

研究简报

三氯化铁催化合成2,3-二氢苯并色原酮

丁晓友, 徐凡   

  1. 苏州大学材料与化学化工学部 苏州 215123
  • 收稿日期:2018-06-06 修回日期:2018-07-30 发布日期:2018-08-23
  • 通讯作者: 徐凡 E-mail:xufan@suda.edu.cn
  • 基金资助:

    国家自然科学基金(No.21272168)资助项目.

Ferric Chloride Catalyzed Synthesis of 2,3-Dihydro-benzo[f]chromen-1-one

Ding Xiaoyou, Xu Fan   

  1. College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123
  • Received:2018-06-06 Revised:2018-07-30 Published:2018-08-23
  • Contact: 10.6023/cjoc201806007 E-mail:xufan@suda.edu.cn
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No. 21272168).

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.

关键词: 三氯化铁, 芳并吡喃酮, 催化, Fries重排, 氢烷氧化反应

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.

Key words: ferric chloride, aromatic-fused pyrone, catalysis, Fries rearrangement, hydroalkoxylation