Conclusions
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1.
A study was made of the acylation of phenol with the hydrochlorides of carboxylic acid amides in nitrobenzene solution.
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2.
The hydrochlorides of the N,N-dialkyl-substituted amides of carboxylic acids possess the highest acylating capacity.
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3.
The formation of the N-protonated form of the amide is apparently one of the possible paths for progress of the acylation reaction.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2590–2594, November, 1970.
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Vinogradova, S.V., Vasnev, V.A., Komarova, L.I. et al. Acylation of phenol with the hydrochlorides of carboxylic acid amides. Russ Chem Bull 19, 2431–2434 (1970). https://doi.org/10.1007/BF00859090
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DOI: https://doi.org/10.1007/BF00859090