• Title of article

    Crystal structure of (1RS,21SR,22RS,24SR)-28-oxo-24-propyl-8,11,14-trioxa-24,27-di­aza­penta­cyclo[19.5.1.122,26.02,7.015,20]octa­cosa-2,4,6,15(20),16,18-hexa­ene acetic acid monosolvate

  • Author/Authors

    Hieu, Truong Hong Institute of Chemistry - Vietnam Academy of Science and Technology, Vietnam , Anh, Le Tuan Department of Chemistry - Vietnam National University, Vietnam , Soldatenkov, Anatoly T. Organic Chemistry Department - Peoples' Friendship University of Russia, Russian Federation , Tuyen, Nguyen Van Institute of Chemistry - Vietnam Academy of Science and Technology, Vietnam , Khrustalevd, Victor N. norganic Chemistry Department - Peoples' Friendship University of Russia, Russian Federation

  • Pages
    12
  • From page
    1
  • To page
    12
  • Abstract
    The title compound, C26H32N2O4(M)·C2H4O2, (I), is the product of the Petrenko–Kritchenko condensation of N-propyl­piperidinone with 1,5-bis­(2-formyl­phen­oxy)-3-oxa­pentane and ammonium acetate. In M, the aza-14-crown-3-ether ring adopts a bowl conformation, with the configuration of the C—O—C—C —O—C—C—O—C polyether chain being t–g(−)–t–t–g(+)–t (t = trans, 180°; g = gauche, ±60°). The dihedral angle between the planes of the benzene rings fused to the aza-14-crown-4-ether moiety is 62.75 (5)°. The central piperidinone ring has a boat conformation, whereas the terminal piperidinone ring adopts a chair conformation. The boat conformation of the central piperidinone ring is supported by the bifurcated intra­molecular N—H⋯O hydrogen bond. In the crystal, each solvent mol­ecule is linked to mol­ecule M via strong O—H⋯N hydrogen bonding, forming hydrogen-bonded pairs of mol­ecules, which further inter­act through weak C—H⋯O hydrogen bonds, forming layers parallel to the ac plane.
  • Keywords
    aza-14-crown-3-ether , crystal structure , Petrenko–Kritchenko condensation
  • Journal title
    Acta Crystallographica Section E: Crystallographic Communications
  • Serial Year
    2016
  • Record number

    2618011