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An efficient protocol for synthesizing dibenzodithiapentalenes
Authors:Tue Heesgaard Jepsen,Mogens LarsenMorten Jø  rgensen,Mogens Brø  ndsted Nielsen
Affiliation:a Discovery Chemistry and DMPK, H. Lundbeck A/S, Ottiliavej 9, DK-2500 Valby, Denmark
b Department of Chemistry, University of Copenhagen, Universitetsparken 5, DK-2100 Copenhagen Ø, Denmark
Abstract:Two new scalable methods for the synthesis of dibenzo[bc,fg]dithiapentalene (2) (DPP) are reported starting from either 1-bromo-3-fluoro-2-iodobenzene over four steps in 57% yield or from THP-protected 3-fluorothiophenol over three steps in 43% yield. Attempts to prepare dibenzodioxapentalene (15) using similar conditions were unsuccessful. Instead, we observed the formation of a macrocyclic dimeric product 16. Fluorine-hydrogen bond interactions were observed by NMR in the F/SH- and F/OH-substituted dibenzothiophene and dibenzofuran intermediates.
Keywords:Dibenzo[bc,fg][1,4]dithiapentalene   Dibenzofuran   Nucleophilic aromatic substitution   Fluorine-hydrogen bonding
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