| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1314651 | Journal of Fluorine Chemistry | 2011 | 7 Pages |
Building on recent results of Umemoto and Winter, an improved method of synthesis of arylsulfur trifluorides, including the excellent, new deoxofluorination reagent Fluolead, is hereby reported. The method utilizes Br2 and KF as oxidizing and fluorinating reagents for efficient, high yield conversion of aryl disulfides and mercaptans to arylsulfur trifluorides. It has also been shown that both Fluolead and mesitylsulfur trifluoride may be generated in acetonitrile and used as in situ deoxofluorination reagents for conversion of either aldehydes or ketones to their respective gem-difluoro compounds. An analysis of the probable mechanism of action, including computational efforts, allows postulation of a rationale for the highly variable reactivities of different arylsulfur trifluorides as deoxofluorination reagents.
Graphical abstractBr2 and KF are utilized as oxidizing and fluorinating reagents for efficient, high yield conversion of aryl disulfides and mercaptans to arylsulfur trifluorides.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Arylsulfur trifluorides are synthesized from thiophenols and aryl disulfides in very good yield. ► Arylsulfur trifluorides are effective in situ deoxofluorination reagents with aldehyde and ketone substrates. ► Calculations help explain variations in reactivity of arylsulfur trifluorides in their deoxofluorination reactions.
