The Reaction of Propiolic Acid Esters with Tertiary Amines. Formation of Betaines

  • McCulloch A
  • McInnes A
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Abstract

Reaction of propiolate esters, H—C≡C—CO 2 R, with tertiary alkylamines R′ 3 N in highly aqueous media yields betaines of the type trans R′ 3 N + •CH=CH•CO 2 − . The spectral and chemical properties of these derivatives are discussed as well as the mechanism of their formation. The major by-product of reaction is the corresponding trans-3-alkoxyacrylate RO—CH=CH—CO 2 R.

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McCulloch, A. W., & McInnes, A. G. (1974). The Reaction of Propiolic Acid Esters with Tertiary Amines. Formation of Betaines. Canadian Journal of Chemistry, 52(21), 3569–3576. https://doi.org/10.1139/v74-534

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