Abstract:CCDC no.: 1522954The asymmetric unit of the title crystal structure is shown in the figure. Tables 1 and 2 contain details of the measurement method and a list of the atoms including atomic coordinates and displacement parameters.
Source of materialsMethyl hydrazinecarboxylate (0.9 g, 10 mmol) and 4-diethylamino-2-hydroxybenzaldehyde (1.93 g, 10 mmol) were dissolved in stirred methanol (25 mL). The reaction mixture was refluxed for 7-8 h with TLC monitoring (ethyl acetate:hexane = 1:1). The resulting solid was… Show more
“…The bond lengths and bond angles are in the normal ranges [6,7]. There is intramolecular hydrogen bonds (for example: O2-H2• • • N2) in the molecules, which is typical for such compounds [8]. The hydrogen bonds O1W-H1WA…”
“…The bond lengths and bond angles are in the normal ranges [6,7]. There is intramolecular hydrogen bonds (for example: O2-H2• • • N2) in the molecules, which is typical for such compounds [8]. The hydrogen bonds O1W-H1WA…”
Benzyl N′-[(E)-2-hydroxybenzylidene]hydrazinecarboxylate, C15H14N2O3 (I) and benzyl N′-[(E)-5-bromo-2-hydroxybenzylidene]hydrazinecarboxylate (II), C15H13BrN2O3, have been synthesized by the reaction of either 2-hydroxybenzaldehyde or 5-bromo-2-hydroxybenzaldehyde with benzyl carbazate, respectively. Both the compounds crystallize in the monoclinic crystal system with space groups Pn (Z′ = 1, I) and P21/c (Z′ = 2, II). Molecular conformations in each structure are similar, and both structures feature strong intramolecular O—H...N hydrogen bonds, which form S(6) ring motifs. There are also strong N—H...O and weak C—H...O hydrogen bonds in both structures, but their modes of packing within their respective crystals are markedly different. Some comparisons are made with the structures of a few related compounds.
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