Conclusions
Dimethylaminoethyl (4-hydroxy-3, 5-ditert-butylphenyl) ketone, in contrast to certain other ketones of a series of sterically hindered phenols, reacts with phenylhydrazine, potassium hydroxide, sodium cyanide, and organic magnesium compounds as a normal β-aminoketone.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 920–922, April, 1968.
The authors thank N.M. Emanuel for his interest in this work in the process of its fulfillment.
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Portnykh, N.V., Volod'kin, A.A. & Ershov, V.V. New functional derivatives of sterically hindered phenols. Russ Chem Bull 17, 886–887 (1968). https://doi.org/10.1007/BF00905779
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DOI: https://doi.org/10.1007/BF00905779