Abstract
Investigations are reported concerning the deprotonation of 1,3-indandione and 2-benzyl- 1,3-indandione and the alkylation of these compounds by benzylbromide. Both reactions are performed in a microemulsion and rate and equilibrium constants are determined. In order to discuss the results, deprotonation and alkylation are also studied in aqueous solution and polar organic solvents, respectively.
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References
Kuck D (1984) Angew. Chemie 94: 515
Kahlweit M, This Volume 1
Davies CW (1962), Ion Association, Butterworths, London.
Hanke VR, Knoche W, Dutkiewicz E (1987) J. Chem. Soc., Faraday Trans. 1 83:2847
Knoche W in: Electrochemical Reaction in Nanaqueous and Mixed Solvants, 8th Symposium of the Electrochemical Section of the Polish Chemical Soecity, Poznan-DymaczeWo, June 1985
Parker AJ (1969) Chemical Reviews 69:1
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© 1989 Springer-Verlag Berlin Heidelberg
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Schomäcker, R., Stickdorn, K., Knoche, W. (1989). Deprotonation and Alkylation of 1,3-Indandiones in a Water/N-Heptane/N-Octyl-Phenyl-Pentaoxyethylene Microemulsion. In: Knoche, W., Schomäcker, R. (eds) Reactions in Compartmentalized Liquids. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-74787-8_4
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DOI: https://doi.org/10.1007/978-3-642-74787-8_4
Publisher Name: Springer, Berlin, Heidelberg
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