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One-pot synthesis of 3-haloflavones from flavones using Oxone® and potassium halide as a halogenation reagent.
- Source :
-
Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry . Feb2020, Vol. 61 Issue 7, pN.PAG-N.PAG. 1p. - Publication Year :
- 2020
-
Abstract
- • 3-Haloflavones were synthesized from the corresponding flavones. • This method use Oxone® and potassium halide as a halogenation reagent. • 3-Chloro, 3-bromo and 3-iodo flavones can be conveniently synthesized. A two-step, one-pot method has been developed for the synthesis of 3-haloflavones from the corresponding flavones. The method uses Oxone® and potassium halide to produce the active molecular halogen in situ. The solvent (methanol) then participates in the reaction to afford the 2-methoxy-3-haloflavanone derivative. After adding sodium hydroxide, the corresponding 3-haloflavone product is obtained in good to excellent yields. This method provides a convenient synthesis of 3-chloro, 3-bromo and 3-iodo flavones from the same flavone starting material. [ABSTRACT FROM AUTHOR]
- Subjects :
- *HALOGENATION
*POTASSIUM
*HALIDES
*SODIUM hydroxide
*FLAVONES
Subjects
Details
- Language :
- English
- ISSN :
- 00404039
- Volume :
- 61
- Issue :
- 7
- Database :
- Academic Search Index
- Journal :
- Tetrahedron Letters: International Organ for the Rapid Publication of Preliminary Communications in Organic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 141435011
- Full Text :
- https://doi.org/10.1016/j.tetlet.2019.151511