Synthesis and Supramolecular Structure of 2-Acetyl-1-naphthol
نویسندگان
چکیده
منابع مشابه
Cyclization of hydrazones of 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene. Synthesis of Spiro naphthoxazine dimers.
Cyclization of hydrazones derived from 2-acetyl-1-naphthol and 1-acetyl-2-naphthol with triphosgene gave naphtho[1,2-e]-1,3-oxazines, naphtho[2,1-e]-1,3-oxazines or their spiro dimers depending on the molar ratio of triphosgene used for the cyclization.
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The title compound, C(11)H(9)NO(2), was prepared by a condens-ation reaction of 2-hydr-oxy-1-naphthaldehyde with hydroxyl-ammonium chloride in refluxing ethanol. An intra-molecular O-H⋯N hydrogen bond is observed. In the crystal structure, inter-molecular O-H⋯O and C-H⋯O hydrogen-bond inter-actions result in a two-dimensional network.
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The Re(I) complexes [Re(HPAN)(CO)(3)Cl], 1, and [Re(2)(PAN)(2)(CO)(6)]·C(6)H(12), 2·C(6)H(12), have been prepared by reacting [Re(CO)(5)Cl] with HPAN. Here (PAN)(-) is the deprotonated form of 1-(2-pyridylazo)-2-naphthol. A subsequent reaction of [Re(HPAN)(CO)(3)(CF(3)SO(3))] with a chelating diphosphine ligand generates [Re(PAN)(CO)(P-P)]·CH(2)Cl(2), 3·CH(2)Cl(2). The structures of the complex...
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The aim of doing this research is a one-pot three-component synthesis of 1-aminoalkyl-2- naphthol and naphthoxazine derivatives using the condensation of β-naphthol with various aldehydes and amines in the presence of ionic liquid {[(secondary butyl) methyl] imidazolium bromide} {[sec-bmim]+ Br-, as an efficient catalyst and solvent. The catalyst was prepared according...
متن کامل6-Bromo-2-naphthol–piperazine (2/1)
In the title compound, 2C(10)H(7)BrO·C(4)H(10)N(2), the piperazine (pip) mol-ecule displays a chair conformation and is linked to two mol-ecules of 6-bromo-2-naphthol (bno) via O-H⋯N hydrogen bonds. Weak N-H⋯O hydrogen bonds from pip to bno mol-ecules result in chains propagating in [100]. The chains inter-act via C-H⋯π inter-actions.
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ژورنال
عنوان ژورنال: Asian Journal of Chemistry
سال: 2013
ISSN: 0970-7077,0975-427X
DOI: 10.14233/ajchem.2013.14314