Summary
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1.
Secondary alcohols react with tetralin in presence of zinc chloride at a lower temperature than primary alcohols do.
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2.
With rise in the molecular weight of the alcohol, the yield of alkyltetralins falls.
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N. I. Shuikin and N. A. Pozdnyak, Izv. AN SSSR, Otd. khim. n.1961, 326.
N. I. Shuikin and N. A. Pozdnyak, Izv. AN SSSR, Otd. khim. n.1961, 1098.
R. H. Pickard and I. Kenyon, J. Am. Chem. Soc.99, 55 (1911).
E. Barraclough et al., Dictionary of Organic Compounds [Russian translation] (IL, Moscow, 1949) Vol. 1, p. 363; Vol. 2, p. 724.
N. I. Shuikin, V. A. Shlyapochnikov, N. A. Pozdnyak, and B. L. Lebedev, Izv. AN SSSR, Otd. khim. n. 1961, 466.
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The infrared spectra were determined by I. N. Lifanova, to whom the authors express their thanks.
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Shuikin, N.I., Pozdnyak, N.A. Catalytic alkylation of tetralin. Russ Chem Bull 11, 301–303 (1962). https://doi.org/10.1007/BF00908040
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DOI: https://doi.org/10.1007/BF00908040