1-Ethoxy-3-[4-(ethoxycarbonyl)phenyl]-3-hydroxy-1-oxopropan-2-aminium chloride

IUCrData Pub Date : 2024-10-01 Epub Date: 2024-10-31 DOI:10.1107/S2414314624010320

Dieter Schollmeyer , Igor Proz , Heiner Detert

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Abstract

The title compound was prepared as a racemate of R,R- and S,S-enantiomers by reduction of the corresponding hydroxyiminoketone. In the crystal, layers are formed via hydrogen bridges of four ammonium groups to chloride ions; these lamellae are connected via interdigitated benzoic ester groups.

The title compound, C₁₄H₂₀NO₅⁺·Cl⁻, was prepared as a racemate of R,R- and S,S-enantiomers by reduction of the corresponding hydroxyiminoketone. In the crystal, layers are formed via hydrogen bridges of four ammonium groups to chloride ions; these lamellae are connected via interdigitated benzoic ester groups.

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