2-Aminophenol

Abstract: Anil compounds are Schiff bases derived from aniline moiety containing phenyl or substituted phenyl group, which sometimes called Azo dyes. These Schiff bases can be directly prepared from aromatic amine with aromatic carbonyl groups, which are stable and can be manipulated under different and suitable conditions. The phenomena of coordination of Schiff bases with metal ions give the Schiff bases the good advantages to be introduced in the dyes synthesis. The classification of dyes is based on the chemical structure or on the basis of the chromophoric system. The metal complex dyes are combinations of dyestuff and metal ions, in which the coordination complex can be applied or used to be improvement factors in dye techniques. The investigation and the characterization of the resulted dyes were performed by using different physical techniques. The produced dyes were applied to different fibres, such as sheep wool and goat hair with two Schiff bases synthesised from salicylaldehyde either with 2-aminophenol or 2-aminobenzyl alcohol. Also the investigation includes the effect of mordant type on the dyeing process.

Abstract: A new tetranitrosyl binuclear iron complex, [Fe2(SC6H6N)2(NO)4] (1), has been synthesized by two methods. Molecular and crystalline structure of 1 were determined by X-ray analysis; the complex is binuclear of “μ-S” type with ~2.7052(4) A between the irons. The compound crystallizes in monoclinic, space group P21/n, Z = 2; parameters of the unit cell: a = 6.6257(2) A, b = 7.9337(2) A, c = 16.7858(4) A, β = 96.742(2)°, V = 876.26(4) A3. Parameters of Mossbauer spectrum for 1 are: isomer shift δFe = 0.096(1) mm/s, quadrupole splitting ΔEQ = 1.122(1) mm/s, line width 0.264(1) mm/s at 293 K. As follows from the electrochemical analysis of aqueous solutions of 1, it generates NO in protonic media without additional activation. NO amount and the rate of its activation are much higher in acidic solutions than in neutral and alkali ones. The constants of hydrolytic decomposition of 1 were calculated. The geometry and electronic structure of isolated 1 were studied using the density functional theory. Differential...

Abstract: A direct coupling of carboxylic acids with 2-aminophenol under microwave irradiation has been achieved leading to the synthesis of 2-substituted benzoxazoles under metal and solvent-free conditions. Aliphatic, aromatic and heteroaromatic carboxylic acids provide good yields. Benzoxazole formation takes place in the presence of chloro, methoxy, phenoxy, thiophenoxy, and α,β-unsaturated functionalities. In the case of dicarboxylic acids, the reaction proceeds via the formation of the corresponding anhydride with predominant formation of the mono-benzoxazole.

Abstract: Lawesson's reagent (LR) reacts with 1,2-phenylenediamine derivatives (2a-c) to give 1,3-dihydro-1,3,2-diazaphosphole-2-sulfide (3a-e). Also it reacts with 2-aminophenol (4) and 2-amino-2-methyl-1-pro-panol (6) to give 1,3,2-oxazaphospholes 5, 7 respectively.