67534-80-9

Upstream product

• 118-93-4 o-hydroxyacetophenone 
• 99-73-0 para-bromophenacyl bromide 
• 3343-45-1 4-bromo-2-hydroxyacetophenone 
• 1422044-74-3 C₁₉H₁₉BrO₂Si 
• 582-24-1 1-phenyl-2-hydroxyethanone 

Downstream Products

• 67534-86-5 (3-bromomethyl-benzofuran-2-yl)-(4-bromo-phenyl)-methanone 

Relevant academic research and scientific papers

Synthesis and antimicrobial evaluation of substituted (1,1'-biphenyl)-4-yl(3-methylbenzofuran-2-yl)methanones by Suzuki cross-coupling reaction

A series of new substituted [1,1'-biphenyl]-4-yl(3-methylbenzofuran-2-yl)methanones was prepared by Suzuki cross-coupling from (4-bromophenyl)(3-methylbenzofuran-2-yl)methanone. The obtained compounds were assayed for their in vitro antibacterial activity against different types of bacterial strains; antifungal activity was also examined by inhibitory effect against different fungal strains.

Bi(OTf)3-Mediated (4+1) Annulation of α-Sulfonyl o-Hydroxyacetophenones with α-Hydroxy Arylketones to Access Sulfonyl 2-Aroylbenzofurans

In this paper, a high-yield, facile route for the scalable synthesis of sulfonyl 2-aroylbenzofurans via a Bi(OTf)3-mediated intermolecular double cyclocondensation of α-sulfonyl o-hydroxyacetophenones with substituted α-hydroxy arylketones under mild open-vessel reaction conditions is described. In the overall reaction, water is generated as the only byproduct. Various metal triflate-promoted reactions and conditions are investigated for the efficient one-pot (4+1) annulation reaction. (Figure presented.).

Solution-phase photochemical transformation of 2-aroylbenzofurans: Addition-elimination mechanism

An efficient conversion of 2-aroylbenzofurans into arylbenzofurylmethanols through photoreduction has been described. In these molecules, the photo transformation occurred through the initial addition of solvent followed by elimination involving γ-hydroge

A highly efficient ultrasound-promoted synthesis of 2,3-disubstituted benzo[b]furans via intramolecular C-C bond formation in ionic liquid[bmim]BF4 at room temperature

An efficient ultrasound-promoted synthesis of 2,3-disubstituted benzo[b]furans in the ionic liquid [bmim]BF4 at room temperature is reported. 5-exo-dig carbanion-yne intramolecular cyclization is mediated using anhydrous K3PO4/

DMAP-catalyzed cascade reaction: One-pot synthesis of benzofurans in water

A series of benzofurans were efficiently synthesized in good to excellent yields using 4-dimethylaminopyridine (DMAP) catalyzed cascade reaction between salicylaldehydes and halogenated ketones in water at 80 °C opened atmosphere.

Benzofuranyl-and thiophenylmethylthio-alcanecarboxylic acid derivatives

Benzofuranyl-and thiophenylmethylthio-alkanecarboxylic acid derivatives are prepared by brominating appropriate methyl compounds and reacting the methyl bromides thus obtained with mercapto-alkanecarboxylic acid derivatives. The new substances are suitabl