Solvolysis of 3,5-Di-tert-butyl-4-hydroxybenzyl Acetate in Alcohol Solutions

Solvolysis of 3,5-di-tert-butyl-4-hydroxybenzyl acetate in alcohol solutions involves intermediate formation of 2,6-di-tert-butyl-4-methylene-1-benzoquinone that further takes up a molecule of the alcohol.     

Reaction of Tetramethylcalix[4]resorcinolarene with 3,5-Di-tert-butyl-4-hydroxybenzyl Acetate

Upper-rim modification of tetramethylcalix[4]resorcinolarene with 3,5-di-tert-butyl-4-hydroxybenzyl fragments is accompanied by unusual decomposition of the macroring in the modified product with formation of 2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)resorcinol.     

Unusual Reaction of Tetramethylcalix[4]resorcinolarene with 3,5-Di-tert-butyl-4-hydroxybenzyl Acetate

Russian Journal of General Chemistry -     

Reactions of 3,5-di-tert-Butyl-4-hydroxybenzyl Acetate with Weakly Basic Nucleophiles

The acid dissociation of 3,5-di-tert-butyl-4-hydroxybenzyl acetate in the presence of bases or in dimethylformamide favors reaction of this compound with weakly basic nucleophilies.     

Crystal and Molecular Structure of 2,4,6-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)resorcinol

The structure of 2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)resorcinol in the crystal is virtually identical to that of 1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)mesitylene, which is an effective antioxidant.     

3,5-Di-tert-butyl-4-hydroxybenzaldehyde derivatives as antioxidants in cumene oxidation

A series of 4-hydroxy-3,5-di-tert-butylbenzaldehyde derivatives were prepared, and their antioxidant properties were studied.     

Reactions of 4-acylresorcinol derivatives with 3,5-di-tert-butyl-4-hydroxybenzyl acetate

Reactions of hydroxyphenylcarbonyl derivatives with 3,5-di-tert-butyl-4-hydroxybenzyl acetate under mild conditions gave novel functionalized diarylmethanes. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1128–1133, July, 2006.     

Reaction of alkyl splitting of 4-acetylamino-N-(3,5-di-tert-butyl-4-hydroxybenzyl)-benzenesulfonamide

Russian Journal of General Chemistry - Alkyl splitting of 4-acetylamino-N-(3,5-di-tert-butyl-4-hydroxybenzyl)benzenesulfonamide with alkali solution has been discovered, the reaction being uncommon...     

Condensation of certain selected 1-monoalkylisoindigo with 3,5-di-tert-butyl-4-hydroxybenzyl acetate

Russian Journal of General Chemistry -     

The Crystal Structure and Intermolecular Interactions in Fenamic Acids–Acridine Complexes

In order to improve pharmaceutical properties of drugs, complexes are synthesized as combinations with other chemical substances. The complexes of fenamic acid and its derivatives, such as mefenamic-, tolfenamic- and flufenamic acid, with acridine were obtained and the X-ray structures were discussed. Formation of the crystals is determined by the presence of the intermolecular O–H^…N hydrogen bond that occur between fenamic acids and acridine. Intermolecular interactions stabilizing the crystals such as π^…π stacking, C–H^…X (X = O, Cl) intermolecular hydrogen bonds as well as C–H^…π and other dispersive interactions were analyzed by theoretical methods: the quantum theory of atoms in molecules (QTAIM) and noncovalent interaction (NCI) approaches.     

Reactions of derivatives of phosphorylacetic acid hydrazides with 3,5-di-tert-butyl-4-hydroxybenzyl acetate

Abstract

To obtain new polyfunctional inhibitors of radical-chain oxidative processes, C- and N-benzylation of a number of phosphorylacetic acid hydrazide derivatives is realized in their reactions with 3,5-di-tert-butyl-4-hydroxybenzyl acetate. N-benzylation of mixtures of Z and E isomers of hydrazones of phosphorylacetic acid derivatives proceeds stereoselectively with the formation of only E_C=N isomers.     

Syntheses and Crystal Structures of 3,5-Diiodo-salicylalidehyde and 3,5-Diiodo-salicylalidene-4-nitroaniline

The title compounds, C7H4I2O2 1 and C13H7I2N2O3 2, have been synthesized and characterized by single-crystal X-ray diffraction. Compound 1 crystallizes in monoclinic, space group P21/c with a = 9.802（2）, b = 13.867（3）, c = 7.364（2） A, β = 109.74（3）°, V= 942.1（3） A^3, Dc= 2.636 g/cm^3, C7H4I2O2, Mr= 373.90, F（000） = 672, μ = 6.627 mm^-1, Z = 4, R = 0.0459 and wR = 0.1018 for 1805 observed reflections （I 〉 2 σ（I））. Compound 2 belongs to the monoclinic system, space group P21/n with a = 9.015（2）, b = 12.024（2）, c = 14.072（3） A, β = 103.91（3）°, V = 1480.6（5） A^3, Dc= 2.216 g/cm^3, C13H7I2N2O3, Mr= 494.01, F（000） = 920, p = 4.255 mm^-1, Z = 4, R = 0.0777 and wR = 0.1757 for 2896 observed reflections （I 〉 2σ（I））. Compounds 1 and 2 were assayed for antibacterial activities against three Gram positive bacterial strains （B. subtilis, S. aureus and S. faecalis） and three Gram negative bacterial strains （E. coli, P. aeruginosa and E. cloacae） by MTr method. Fortunately, compound 2 is found to show potent antibacterial activity against these six bacterial strains.     

New Data on the Reaction of Diethyl Hydrogen Phosphite with 3,5-Di-tert-butyl-4-hydroxybenzaldehyde

3,3',5,5'-Tetra-tert-butylstilbene quinone and 1,2-bis(3,5-di-tert-butyl-4-hydroxyphenyl)-1,2-bis-(diethoxyphosphinoyl)-ethane were isolated from a mixture of products of the reaction of equivalent amounts of diethyl hydrogen phosphite and 3,5-di-tert-butyl-4-hydroxybenzaldehyde. A scheme of chemical transformations in this reaction system was offered.     

Synthesis of hybrid compounds by benzylation of acylhydrazones with 3,5-di-tert-butyl-4-hydroxybenzyl acetate

Russian Chemical Bulletin - N-Benzylation of acylhydrazones of the hydroxybenzaldehyde series with 3,5-di-tert-butyl-4-hydroxybenzyl acetate was performed at room temperature in the absence of acid...     

Oxidation of Group II Metals with 3,5-Di-tert-butyl-1,2-benzoquinone

Kinetic regularities of zinc and cadmium oxidation in systems comprising 3,5-di-tert-butyl-1,2-benzoquinone and dimethylformamide or dimethyl sulfoxide are studied. Thermodynamic parameters of oxidant and ligand adsorption on metal surface are estimated. The oxidation of Group II metals (Be, Ca, Mg, Zn, Cd) with 3,5-di-tert-butyl-1,2-benzoquinone gives metal bis-o-semiquinolates. In the presence of excess metal in the medium of coordinating solvents, diradical products convert to the corresponding catecholate derivatives. It is shown that the dependence of the rates of metal reactions with 3,5-di-tert-butyl-1,2-benzoquinone on the donor number of solvent passes through a maximum. With less active metals, the maximum shifts to more basic ligands.