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Synthesis 1990; 1990(7): 569-570
DOI: 10.1055/s-1990-26942
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An Improved Synthetic Method for dl-Griseofulvin and Its 2′-S-Analogue

Masatoshi Yamato* , Yasuo Takeuchi, Hideo Tomozane
  • *Faculty of Pharmaceutical Sciences, University of Okayama, Tsushima-naka 1-1-1, Okayama 700, Japan
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Publikationsdatum:
17. September 2002 (online)

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An improved synthetic method for dl-giseofulvin (4) and its 2′-S-analogue 8 has been developed. 7-Chloro-4,6-dimethoxy-2-[5-methoxy-1-methylthio-3-oxohexylidene]-3 (2H)-benzofuranone (7), prepared by reaction of the corresponding 3 (2H) -benzofuranone with 1,1-bis(methylthio)-5-methoxy-1-hexen-3-one (6), undergoes stereoselective intramolecular cyclization when treated with activated alumina in refluxing diethyl ether. The product, the 2′-S-analogue of dl-griseofulvin 8, is converted to dl-griseofulvin (4) in good yield.