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The ferric chloride test is used to determine the presence of phenols in a given sample or compound (for instance natural phenols in a plant extract). Enols, hydroxamic acids, oximes, and sulfinic acids give positive results as well. [1]
The reaction is attractive for their atom economy because it avoid pre-functionalized starting materials often required in traditional redox-neutral cross-couplings. Oxidative phenol couplings, however, often suffer from over-oxidation, especially since the intended coupled product is more oxidizable (has a lower oxidation potential ) than the ...
A few types of aromatic compounds, such as phenol, will react without a catalyst, but for typical benzene derivatives with less reactive substrates, a Lewis acid is required as a catalyst. Typical Lewis acid catalysts include AlCl 3 , FeCl 3 , FeBr 3 and ZnCl 2 .
Phenol esters are active esters, being prone to hydrolysis. Phenols are reactive species toward oxidation. Oxidative cleavage, for instance cleavage of 1,2-dihydroxybenzene to the monomethylester of 2,4 hexadienedioic acid with oxygen, copper chloride in pyridine [4] Oxidative de-aromatization to quinones also known as the Teuber reaction.
The first stage of Fenton's reaction (oxidation of Fe 3+ with hydrogen peroxide) is used in Haber–Weiss reaction; Fenton's reagent can be used in organic synthesis reactions: e.g. hydroxylation of arenes via a free radical substitution; Conversion of benzene into phenol by using Fenton's reagent; Oxidation of barbituric acid into alloxan.
Iron(III) chloride forms a 1:2 adduct with Lewis bases such as triphenylphosphine oxide; e.g., FeCl 3 (OP(C 6 H 5) 3) 2. The related 1:2 complex FeCl 3 (OEt 2) 2, where Et = C 2 H 5), has been crystallized from ether solution. [14] Iron(III) chloride also reacts with tetraethylammonium chloride to give the yellow salt of the tetrachloroferrate ...
Phenol is an organic compound appreciably soluble in water, with about 84.2 g dissolving in 1000 ml (0.895 M).Homogeneous mixtures of phenol and water at phenol to water mass ratios of ~2.6 and higher are possible.
To a stirred solution of p-(3-hydroxypropyl)phenol (152 mg, 1 mmol) and pyridine (0.3 mL) in acetonitrile (10 mL) at 0° was added a solution of IBTA (430 mg, 1 mmol) in acetonitrile (2 mL). The mixture was stirred at room temperature for 10 minutes, diluted with water, and extracted with diethyl ether (3 × 10 mL).