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Oxidative fluorination with Selectfluor: A convenient procedure for preparing hypervalent iodine(V) fluorides.
Dearman, Samuel M G; Li, Xiang; Li, Yang; Singh, Kuldip; Stuart, Alison M.
Affiliation
  • Dearman SMG; School of Chemistry, University of Leicester, Leicester, LE1 7RH, UK.
  • Li X; School of Chemical Engineering, Dalian University of Technology, No. 2 Linggong Road, Dalian, 116024, P. R. China.
  • Li Y; School of Chemical Engineering, Dalian University of Technology, No. 2 Linggong Road, Dalian, 116024, P. R. China.
  • Singh K; School of Chemistry, University of Leicester, Leicester, LE1 7RH, UK.
  • Stuart AM; School of Chemistry, University of Leicester, Leicester, LE1 7RH, UK.
Beilstein J Org Chem ; 20: 1785-1793, 2024.
Article in En | MEDLINE | ID: mdl-39109295
ABSTRACT
The ability to investigate hypervalent iodine(V) fluorides has been limited primarily by their difficult preparation traditionally using harsh fluorinating reagents such as trifluoromethyl hypofluorite and bromine trifluoride. Here, we report a mild and efficient route using Selectfluor to deliver hypervalent iodine(V) fluorides in good isolated yields (72-90%). Stability studies revealed that bicyclic difluoro(aryl)-λ5-iodane 6 was much more stable in acetonitrile-d 3 than in chloroform-d 1, presumably due to acetonitrile coordinating to the iodine(V) centre and stabilising it via halogen bonding.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Beilstein J Org Chem Year: 2024 Document type: Article Country of publication: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Beilstein J Org Chem Year: 2024 Document type: Article Country of publication: Germany