Difluoromethyl (2-benzothiazolyl) sulfone basic information
Chinese name: difluoromethyl (2-benzothiazolyl) sulfone
Difluoromethyl (2-benzothiazolyl) sulfone; 2-((difluoromethyl) sulfonyl) benzo [D] thiazole; 2-[(difluoromethyl) sulfonyl] benzothiazole; Difluoromethylbenzothiazolsulfone; (2)-(difluoromethyl) sulfonyl benzothiazole (D); 3-difluoromethyl sulfone benzothiazole; 2-difluoromethyl sulfone benzothiazole; 2-fluoromethyl sulfone benzothiazole
English name: 2-((Difluoromethyl)sulfonyl)benzo[d]thiazole,98%
2-(Difluoromethyl)sulfChemicalbookonyl)benzo[d]thiazole,98%; 2-[(Difluoromethyl)sulfonyl]benzothiazole; Benzothiazole,2-[(difluoromethyl)sulfonyl]-; 2-Benzo[d]thiazolyldifluoromethylsulfone
CAS number: 186204-66-0
Molecular formula: C8H5F2NO2S2
Molecular weight: 249.26
Related category: Chemical raw materials
Mol File: 186204-66-0.mol
Visible-light induced photocatalyst-free difluoromethylation of quinoxalinones with difluorosulfones[Green Synthesis and Catalysis, 2023]
Abstract
Visible-light induced direct C–H difluoromethylation of quinoxalinones with 2-((difluoromethyl)sulfonyl)benzo[d]thiazole has been developed for the first time. A broad range of quinoxalinones were well tolerated and reacted with difluorosulfone smoothly to give the corresponding products in moderate to good yields. Notably, no external photocatalyst or oxidant was required, which provides a practical and green protocol to access difluoromethylated quinoxalinones. Finally, the control experiments demonstrated a radical mechanism, and the density functional theory (DFT) calculations indicated the radicals were generated through the formation of an electron donor−acceptor (EDA) complex.
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