FACILE SUBSTITUTION REACTION BETWEEN NONACTIVATED ARYL IODIDES AND ARENETHIOLATES IN THE PRESENCE OF COPPER(I) IODIDE

Authors:

5 November 1980

journal article
research article
Published by Oxford University Press (OUP) in Chemistry Letters

Vol. 9 (11) , 1363-1364
DOI:10.1246/cl.1980.1363

Abstract

In hexamethylphosphoric triamide containing copper (I) iodide, nonactivated aryl iodides undergo a facile nucleophilic attack by arenethiolate ions to give the corresponding aryl sulfides in good yields.

Keywords

COPPER
SUBSTITUTION REACTION
ARYL SULFIDES
NUCLEOPHILIC ATTACK
NONACTIVATED
FACILE SUBSTITUTION
IODIDES UNDERGO
ARENETHIOLATE IONS

This publication has 2 references indexed in Scilit:

Copper-promoted reactions in aromatic chemistry
Quarterly Reviews, Chemical Society, 1965
Thioethers from Halogen Compounds and Cuprous Mercaptides. II
Journal of the American Chemical Society, 1959