Issue 0, 1967

Alkyl–oxygen heterolyses in 4-arylpiperidin-4-ols and related esters. Part III. Some 4-alkoxy-4-arylpiperdines

Abstract

The acid-catalysed etherification of some 4-arylpiperidin-4-ols (and esters) is reported and the greater reactivity of cis, compared with trans(3-Me,4-Ph).3-methyl analogues demonstrated. 4-Alkoxypiperidine syntheses of the Williamson type and by the ring opening of 4-piperidone ethylene ketals with phenylmagnesium bromide are also described.

Article information

Article type
Paper

J. Chem. Soc. C, 1967, 979-983

Alkyl–oxygen heterolyses in 4-arylpiperidin-4-ols and related esters. Part III. Some 4-alkoxy-4-arylpiperdines

A. F. Casy and P. Pocha, J. Chem. Soc. C, 1967, 979 DOI: 10.1039/J39670000979

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