An efficient protocol for synthesizing dibenzodithiapentalenes |
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Authors: | Tue Heesgaard Jepsen,Mogens LarsenMorten Jø rgensen,Mogens Brø ndsted Nielsen |
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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 |
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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. |
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Keywords: | Dibenzo[bc,fg][1,4]dithiapentalene Dibenzofuran Nucleophilic aromatic substitution Fluorine-hydrogen bonding |
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