ChemNet
 
Previous article Next article Contents  

R. A. Gazzayeva, A. D. Tsargasov, A. N. Fedotov, S. S. Mochalov

The behavior of the cyclopropyl phenyl sulfide and phenoxycyclopropane in the reaction with nitrous acid

Abstract

The behavior of the cyclopropyl phenyl sulfide and phenoxycyclopropane in the nitrosation reaction was studied. Cyclopropyl phenyl sulfide was found to convert quantitatively to cyclopropyl phenyl sulfoxide under the action of nitrous acid formed in situ. Under the same conditions phenoxycyclopropane undergo transformation to 5-phenoxyisoxasoline (nitrophenols are formed as side products in this reaction).
Moscow University Chemistry Bulletin.
2011, Vol. 52, No. 5, P. 372
   

Copyright (C) Chemistry Dept., Moscow State University, 2002
   Overview
   Editorial board
   Tables of Contents
   Subscription

The site is supported by Russian Foundation for Basic Research
  The using of published on this page materials is not allowed without special permission
Copyright (C) Chemisty Department of Moscow State University
Web-Editor: B.I.Pokrovskii
Web-design: Copyright (C) MIG and VVM
webmaster@www.chem.msu.su