Issue 0, 1967

β-Aroylpropionic acids. Part XXI. The Fries rearrangement of chlorophenyl hydrogen succinates

Abstract

Ortho-, meta-, and para-chlorophenyl hydrogen succinate were subjected to the Fries rearrangement in both 1,1,2,2-tetrachloroethane and toluene. The products were identified by comparison with authentic specimens and by infrared spectroscopy.

The Friedel–Crafts reaction between o-, m-, and p-chloroanisole and o-chlorophenol and succinic anhydride was investigated.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 343-346

β-Aroylpropionic acids. Part XXI. The Fries rearrangement of chlorophenyl hydrogen succinates

F. G. Baddar, I. Enayat and S. M. Abdel-Wahab, J. Chem. Soc. C, 1967, 343 DOI: 10.1039/J39670000343

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