Acids hydroxamic

Folkers J P, Gorman C B, Laibinis P E, Buchholz S and Whitesides G M 1995 Self-assembled monolayers of long-chain hydroxamic acids on the native oxides of metals Langmuir 813-24... 

As esters are usually difficult to detect, this test is of considerable value. In general esters react when heated with hydroxylamine to give a hydroxamic acid (I). The latter gives a coloured complex (II) with ferric salts in acid solution. 

Hydroxamic acid formation resembles amide formation (pp. 117-119) and therefore certain other classes of substances will respond to the test, e.g., acid chlorides and acid anhydrides, but these substances are readily distinguished by other reactions. 

Esters form hydroxamic acids which give colorations with ferric chloride. 

Hydroxamic acid formation cf. Section 9, p. 334). To a few drops of an ester, add 0 2 g. of hydroxylamine hydrochloride and about 5 ml. of 10% NaOH solution and gently boil the mixture for 1-2 minutes. Cool and acidify with dil. HCl and then add a few drops of ferric chloride solution. A violet or deep red-brown colour develops immediately. 

Acid chlorides and anhydrides give hydroxamic acids with... 

Hydroxamic acid formation. To 0 1 g. of acetic anhydride, add 0 1 g. of hydroxylamine hydrochloride and 5 ml. of 10% NaOH solution. Boil the mixture for i minute, cool and acidify with dilute... 

Both succinic and phthalic anhydride respond to the hydroxamic acid test (see 5 above). 

Esters react witli hydroxylamine to form an alcohol and a hydroxamic acid, RCONHOH. All hydroxamic acids, in acid solutions, react with ferric chloride to form coloured (usually violet) complex salts ... 

Lactones, which may be regarded as cyclic or inner esters, react similarly. Anhydrides of carboxylic acids also react with hydroxylamine to form hydroxamic acids ... 

It may be noted that primary aliphatic amides are readily converted by hydro-xylamlne hydrochloride into hydroxamic acids, which may be detected by the addition of ferric chloride solution ... 

Acyl derivatives, RCO—NH—OH and HjN—O—CO—R, are named as A-hydroxy derivatives of amides and as O-acylhydroxylamines, respectively. The former may also be named as hydroxamic acids. Examples are A-hydroxyacetamide for CH3CO—NH—OH and O-acetylhydrox-ylamine for HjN—O—CO—CH3. Further substituents are denoted by prefixes with O- and/or A-locants. For example, C5H5NH—O—C2H5 would be O-ethyl-A-phenylhydroxylamine or A-ethox-ylaniline. 

Salts of thiols (170) or of sulfinic acids (171) react like the alkoxides, giving 4-alkylthio- or 4-alkylsulfono-substituted butyrates. Alkali cyanides give 4-cyanobutyrates (172), hydroxylamine gives a hydroxamic acid (173), and hydra2ine a hydra2ide (174). 

Acid Hydrolysis. With hot concentrated mineral acids, primary nitroparaffins yield a fatty acid and a hydroxylamine salt. If anhydrous acid and lower temperatures are used, the intermediate hydroxamic acid can be recovered. 

The acid chloride of i i7-nitromethane, CH2=N(C1)0 (mp —43°C, bp 2—3°C), is formed by fusion of nitromethane and picrylpyridinium chloride (36). It is hydroly2ed to nitro some thane, reduces potassium permanganate strongly, and exhibits no reactions characteristic of hydroxamic acids. 

The hydrogenolysis of hydroxamic acids (22) and hydra2ides (23) has also been used to synthesi2e amides. One of the earliest methods for the preparation of amides consists of treating acid chlorides with dry ammonia or an amine (24). 

If primary or secondary amines are used, A/-substituted amides are formed. This reaction is called aminolysis. Hydra2ines yield the corresponding hydra2ides, which can then be treated with nitrous acid to form the a2ides used in the Curtius rearrangement. Hydroxylamines give hydroxamic acids. 

Ring substituents show enhanced reactivity towards nucleophilic substitution, relative to the unoxidized systems, with substituents a to the fV-oxide showing greater reactivity than those in the /3-position. In the case of quinoxalines and phenazines the degree of labilization of a given substituent is dependent on whether the intermediate addition complex is stabilized by mesomeric interactions and this is easily predicted from valence bond considerations. 2-Chloropyrazine 1-oxide is readily converted into 2-hydroxypyrazine 1-oxide (l-hydroxy-2(l//)-pyrazinone) (55) on treatment with dilute aqueous sodium hydroxide (63G339), whereas both 2,3-dichloropyrazine and 3-chloropyrazine 1-oxide are stable under these conditions. This reaction is of particular importance in the preparation of pyrazine-based hydroxamic acids which have antibiotic properties. 

Most of the naturally-occurring pyrazine hydroxamic acids appear to be derived from valine, leucine and isoleucine, and biosynthetic studies by MacDonald and coworkers (61JBC(236)512, 62JBC(237)1977, 65JBC(240)1692) indicate that these amino acids are incorporated. However, it would seem that the logical intermediates, viz. the 2,5-dioxopiperazines such as (111) and (112), are not always incorporated. This does not rule out their intermediacy, as there may be problems such as low solubility or membrane permeability which prevent their efficient incorporation. An exception to these results was reported for pulcherrimic acid (113) (65BJ(96)533), which has been shown to be derived from cyclo-L-leu-L-leu which serves as an efficient precursor. 

No simple pteridine 1- or 3-oxides are yet known. If the AT-atom of an amide function is formally oxidized, tautomerism favours the cyclic hydroxamic acid structure, as found for 3-hydroxypteridin-4-one (55JA3927), 1-hydroxylumazine (64JOC408) and 2,4-diamino-8-hydroxypteridin-7-ones (75JOC2332). 

Earlier reported syntheses have been shown to give isoxazolin-5-ones. Other isoxazolin-3-ones have been prepared by the reaction of methylacetoacetic esters and hydroxylamine. An additional synthesis was reported by the action at 0°C of hydroxylamine on ethyl -benzoylpropionate to produce an insoluble hydroxamic acid which cyclized on acid treatment. The hydroxamic acid acetal was similarly transformed into the isoxazolin-3-one (Scheme 149) (71BSF3664, 70BSF1978). 

The use of dehydrating agents such as sulfuric or phosphoric acid on (555 X = OH) was also successful, and these closures may proceed via mixed anhydrides 67AHC(8)277, 75MIP41600). Carbonyldiimidazole effected the conversion of hydroxamic acid (557) into a 3-hydroxy-1,2-benzisoxazole derivative (79JHC1277). The mixed anhydride (558) where... 

THERMODYNAMIC STUDIES ON THE PROTONATION EQUILIBRIA OF SOME HYDROXAMIC ACIDS IN NaNOj SOLUTIONS IN WATER AND IN MIXTURES OF WATER AND DIOXANE... 

The protonation equilibria for nine hydroxamic acids in solutions have been studied pH-potentiometrically via a modified Irving and Rossotti technique. The dissociation constants (p/fa values) of hydroxamic acids and the thermodynamic functions (AG°, AH°, AS°, and 5) for the successive and overall protonation processes of hydroxamic acids have been derived at different temperatures in water and in three different mixtures of water and dioxane (the mole fractions of dioxane were 0.083, 0.174, and 0.33). Titrations were also carried out in water ionic strengths of (0.15, 0.20, and 0.25) mol dm NaNOg, and the resulting dissociation constants are reported. A detailed thermodynamic analysis of the effects of organic solvent (dioxane), temperature, and ionic strength on the protonation processes of hydroxamic acids is presented and discussed to determine the factors which control these processes. 

Me3Si)2NH, Me3SiCl, Pyr, 20°, 5 min, 100% yield. ROH is a carbohydrate. Hexamethyldisilazane (HMDS) is one of the most common sily-lating agents and readily silylates alcohols, acids, amines, thiols, phenols, hydroxamic acids, amides, thioamides, sulfonamides, phosphoric amides, phosphites, hydrazines, and enolizable ketones. It works best in the presence of a catalyst such as X-NH-Y, where at least one of the group X or Y is electron-withdrawing. ... 

Succinyl coenzyme A trisodium salt [108347-97-3] M 933.5. If it should be purified further then it should be dissolved in H2O (0.05g/mL) adjusted to pH 1 with 2M H2SO4 and extracted several times with Et20. Excess Et20 is removed from the aqueous layer by bubbling N2 through it and stored frozen at pH 1. When required the pH should be adjusted to 7 with dilute NaOH and used within 2 weeks (samples should be frozen). Succinyl coenzyme A is estimated by the hydroxamic acid method [J Biol Chem 242 3468 1967]. It is more stable in acidic than in neutral aqueous solutions. [Methods Enzymol 128 435 7956.]... 

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