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Aluminium chloride, a new reagent for the condensation of β-ketonic esters with phenols

Part VI. The condensation of resacetophenone with ethyl α-alkyl-acetoacetates

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Summary

The condensation of resacetophenone with several α-substituted acetoacetates with anhydrous aluminium chloride as condensing agent has been investigated. Ethyl α-methyl-, α-ethyl-, α-benzyl-acetoacetates undergo the condensation with the formation of 5-hydroxy-6-acetyl-3-alkyl-coumarin derivatives. Negative results were obtained with ethyl α-prophyl-, α-allyl, α-chloro-acetoacetates, the original ketone being recovered. The results obtained have been discussed.

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References

  1. Sethana, Shah and ShahJ., 1938, 228.

  2. Shah and ShahIbid., J., 1938, 1424.

  3. Deliwala and ShahIbid. J., 1939, 1250.

  4. Proc. Ind. Acad. Sci., 1941,13 A, 352.

    Google Scholar 

  5. Collie and ChrystallJ., 1907,91, 1804.Ibid., J., 1907,91, 1804.

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  6. Desai and HamidProc. Ind. Acad. Sci., 1938,8,A, 567.

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  7. Sethna and ShahJ. Indian C. S., 1938,15, 383.

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(Communicated by Prof. R.C. Shah, M.SC., Ph.D., F.N.I., F.A.SC.)

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Deliwala, C.V., Shah, N.M. Aluminium chloride, a new reagent for the condensation of β-ketonic esters with phenols. Proc. Indian Acad. Sci. (Math. Sci.) 17, 7–10 (1943). https://doi.org/10.1007/BF03048844

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  • DOI: https://doi.org/10.1007/BF03048844

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