β-Aroylpropionic acids. Part XXI. The Fries rearrangement of chlorophenyl hydrogen succinates
Journal of the Chemical Society C: Organic Pub Date: DOI: 10.1039/J39670000343
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.
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Journal Name：Journal of the Chemical Society C: Organic
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CAS no.: 89640-58-4
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