NaNO2/K2S2O8-mediated selective transformation of 3-formylchromones to 2-hydroxyiminobenzofuran-3-ones and 2-alkoxy-3-(hydroxyimino)chromanones. (8th October 2022)

• Record Type: Journal Article
• Authors: Zheng, Jun; Shoberu, Adedamola; Zhou, Peng-Jun; Sun, Wang-Bin; Ying, Li; Zou, Jian-Ping
• Is Part Of: Tetrahedron. Volume 124(2022)
• Publication Date: 2022-10-08
• Subjects: 3-Formylchromones -- Nitro radical -- Deformylation -- 2-Hydroxyiminobenzofuran-3-ones -- 2-Alkoxy-3-(hydroxyimino)-chromanones; Chemistry, Organic -- Periodicals; 547.005
• DOI: 10.1016/j.tet.2022.133010
• Languages: English
• ISSNs: 0040-4020

Abstract

Abstract: NaNO2 /K2 S2 O8 -mediated deformylative oximation ring contraction (DORC) or deformylative alkoxyoximation (DAO) bifunctionalization reactions of 3-formylchromones under benign conditions are described. The DORC of 3-formylchromones takes place in the presence of K2 S2 O8, NaNO2 and H2 O to give 2-hydroxyiminobenzofuran-3-ones, while the DAO features the bifunctionalization of 3-formylchromones in the presence of K2 S2 O8, NaNO2 and ROH (alcohol) to afford 2-alkoxy-3-(hydroxyimino)chromanones. The preliminary mechanistic studies indicate that NO + NO3 − (one form of NO2 radical dimer) initially adds to the electron-rich C3 -site of 3-formylchromones to form a cationic intermediate, followed by attack of a nucleophile such as H2 O or ROH to form a hemiacetal or acetal intermediate. Subsequently, the hemiacetal undergoes a tandem deformylation, ring-opening and ring-closing process to give 2-hydroxyiminobenzofuran-3-ones, while the acetal undergoes deformylation to give 2-alkoxy-3-(hydroxyimino)chromanones. Graphical abstract: Image 1 Highlights: Reaction of 3-formylchromones, NaNO2, and H2 O or alcohols afforded the products 2-hydroxyiminobenzofuran-3-ones or 2-alkoxy-3-(hydroxyimino)chromanones.