Webpentafluoroethylation of benzoic acid chloride has been computed using 14 different DFT methods. These computed Gibbs energy profiles have been employed to build kinetic models predicting the final product concentration in solution. The best results are obtain ed with the D3-dispersion corrected B3LYP functional, Web21. apr 2024 · The TMSCF 3-derived CuCF 2 CF 3 species has been successfully applied in pentafluoroethylation of organoboronates and terminal alkynes. By using 1,10 …
Pentafluoroethylation of Carbonyl Compounds Using HFC-125 in a …
WebA highly efficient Zn-catalyzed alkylation of ketones and aldimines with Grignard reagents via trialkylzinc (II) ate complexes minimizes problems with the use of only Grignard … WebAn improved synthesis of BIX-C 2 F 5 was described by Shen and coworkers who described it as a “shelf-stable reagent for pentafluoroethylation” [241] of different substrates. The improvement consisted of utilizing 1-fluoro-1,3-dihydro-3,3-dimethyl-1,2-benziodoxole as the starting material with TMSCF 2 CF 3, successfully obtaining BIX-C 2 F 5 in 78% yield. In … clan work culture
From C 1 to C 2 : TMSCF 3 as a Precursor for Pentafluoroethylation
Web1. okt 2024 · A highly efficient copper-mediated aromatic pentafluoroethylation method using TMSCF 3 as the sole fluoroalkyl source is described. The reaction proceeds by a key C 1 to C 2 process, that is, the generation of CuCF 3 from TMSCF 3, followed by a subsequent spontaneous transformation into CuC 2 F 5.Various aryl iodides were … Web17. jan 2024 · It was found that DBU can promote the decomposition of difluorocarbene to give fluoride which then reacts with difluorocarbene to a trifluoromethyl anion. Both electron-rich and electron-deficient substrates were converted to the corresponding analogues in moderate to good yields, without producing byproducts from a pentafluoroethylation. Web16. mar 2024 · We developed 2-position-selective, direct C-H trifluoromethylation, pentafluoroethylation, and heptafluoropropylation of quinoline derivatives. Regioselective transformation was achieved without derivatization of the quinolines. The reaction proceeded at room temperature with high functional group tolerance, even in gram scale. clan wont gain infamy arcane odyssey