SYNTHESIS OF 10,10-DIOXO-10λ6-PHENOXATHIIN DERIVATIVES BY REACTION OF 4,4'-OXYDIBENZOIC ACID WITH SULFUR-CONTAINING ELECTROPHILES
DOI:
https://doi.org/10.1007/1900Keywords:
aromatic dicarboxylic acids, 4, 4'-oxydibenzoic acid, phenoxathiin, polycyclic compounds, cyclization, electrophilic substitutionAbstract
A method for the synthesis of 4-substituted derivatives of 10,10-dioxo-10λ6-phenoxathiin-2,8-dicarboxylic acid by the reaction of 4,4'-oxydibenzoic acid with strong sulfur-containing electrophiles was developed. The interaction with chlorosulfonic acid or oleum was shown to produce a phenoxathiin ring by initial substitution of hydrogen at positions 2 and 2' followed by intramolecular cyclization to 4‑chlorosulfonyl(sulfo)-10,10-dioxo-10λ6-phenoxathiin-2,8-dicarboxylic acid. Using an analogous approach, methods for the synthesis of 4-nitro- and 4,6-dinitro-10,10-dioxo-10λ6-phenoxathiin-2,8-di-carboxylic acids were developed.
How to Cite
Yashchenko, V. S.; Pap, A. A.; Kalechits, G. V.; Makey, A. V.; Ol'khovik, V. K. Chem. Heterocycl. Compd. 2015, 50, 1471. [Khim. Geterotsikl. Soedin. 2014, 1596.]
For this article in the English edition see DOI 10.1007/s10593-014-1612-2