In 2022,Le Vaillant, Franck; Mateos Calbet, Ana; Gonzalez-Pelayo, Silvia; Reijerse, Edward J.; Ni, Shengyang; Busch, Julia; Cornella, Josep published an article in Nature (London, United Kingdom). The title of the article was 《Catalytic synthesis of phenols with nitrous oxide》.Reference of 1-Bromo-3-iodobenzene The author mentioned the following in the article:
Here, an insertion of N2O into a Ni-C bond under mild conditions (room temperature, 1.5-2 bar N2O) for delivering valuable phenols ROH (R = Ph, 4-cyanophenyl, 1-oxo-2,3-dihydro-1H-inden-4-yl, quinolin-6-yl, etc.) and releasing benign N2 was reported. This fundamentally distinct organometallic C-O bond-forming step differs from the current strategies based on reductive elimination and enables an alternative catalytic approach for the conversion of aryl halides RX (X = I, Br) to phenols. The process was rendered catalytic by means of a bipyridine-based ligands for the Ni center. The method is robust, mild and highly selective, and able to accommodate base-sensitive functionalities as well as permitting phenol synthesis from densely functionalized aryl halides. Although this protocol does not provide a solution to the mitigation of N2O emissions, it represents a reactivity blueprint for the mild revalorization of abundant N2O as an O source. In the part of experimental materials, we found many familiar compounds, such as 1-Bromo-3-iodobenzene(cas: 591-18-4Reference of 1-Bromo-3-iodobenzene)
1-Bromo-3-iodobenzene(cas: 591-18-4) has been used in the preparation of 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodec-1-ene and 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene.Reference of 1-Bromo-3-iodobenzene
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com