Iodination of Benzene with Iodine and Metal Salts in Acidic Solvents
- 1 May 1985
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 58 (5), 1611-1612
- https://doi.org/10.1246/bcsj.58.1611
Abstract
Iodobenzene was obtained by a reaction of benzene with molecular iodine in trifluoromethanesulfonic acid in oxygen atmosphere in the presence of vanadium salt as a catalyst. The method affords a new aromatic iodination process in which benzene is iodinated directly with molecular iodine.This publication has 6 references indexed in Scilit:
- The Iodination of Benzene with Iodine in the Thallium(III) Trifluoroacetate-Trifluoroacetic Acid SystemBulletin of the Chemical Society of Japan, 1974
- Aromatic Bromination and Iodination with Mixtures of Antimony (V) Chloride and HalogensBulletin of the Chemical Society of Japan, 1974
- Thallium in organic synthesis. XXII. Electrophilic aromatic thallation using thallium(III) trifluoroacetate. Simple synthesis of aromatic iodidesJournal of the American Chemical Society, 1971
- Halogenation with copper(II) halides. Synthesis of aryl iodidesThe Journal of Organic Chemistry, 1970
- Iodination with electrolytically generated iodine(I)Journal of the American Chemical Society, 1970
- Iodination of aromatic compounds with a mixture of peroxyacetic acid and iodineTetrahedron, 1964