Issue 16, 1969

Silicon disulphide and boron sulphide in the preparation of thiones and pyranthiones

Abstract

Silicon disulphide and boron sulphide can be used with advantage instead of phosphorus pentasulphide for converting non-enolisable ketones, 2-pyrones and 4-pyrones into the corresponding thiones. Of the three reagents, boron sulphide is the most active and is often effective at ordinary temperatures. A convenient synthesis of 3,4-benzocoumarin is noted.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 2192-2195

Silicon disulphide and boron sulphide in the preparation of thiones and pyranthiones

F. M. Dean, J. Goodchild and A. W. Hill, J. Chem. Soc. C, 1969, 2192 DOI: 10.1039/J39690002192

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