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A method was developed for the preparation of acetoxyacetaldehyde (60% yield) by the hydrolysis of 1-ethoxy-1, 2-diacetoxyethane. Acetoxyacetaldehyde oligomerizes even at room temperature.

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Literature cited

  1. B. S. Gorton and J. A. Reeder, J. Org. Chem.,27, 2920 (1962).

    Google Scholar 

  2. N. V. Kuznetsov and Yang Che-min, Izv. Akad. Nauk SSSR, Ser. Khim., 710 (1962).

  3. R. Criegee, Angew. Chem.,70, 173 (1958).

    Google Scholar 

  4. R. Criegee, Chem. Ber.,90, 1070 (1957).

    Google Scholar 

  5. F. Bohlmann, C. Zdero, and W. Gordon, Chem. Ber.,100, 1193 (1967).

    Google Scholar 

  6. U. Sakae, L. Rgodzo, and J. Katsuhiko, J. Chem. Soc. Japan, Pure Chem. Sect.,87, 986 (1966).

    Google Scholar 

  7. J. Furukawa and T. Saegusa, Polymerization of Aldehydes and Oxides, Wiley (1963).

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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 7, pp. 1630–1631, July, 1976.

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Keiko, N.A., Musorina, T.N., Tkacheva, I.A. et al. Synthesis of acetoxyacetaldehyde. Russ Chem Bull 25, 1545–1546 (1976). https://doi.org/10.1007/BF00920840

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  • DOI: https://doi.org/10.1007/BF00920840

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