Aromatic diazonium salts

Aiomatic aisonic acids aie generally prepared by tiie Bart reaction from an aromatic diazonium salt and sodium arsenite ... 

The aza-transfer reaction between 3-hydrazinopyridazines and aromatic diazonium salts or heterocyclic diazo compounds affords the corresponding tetrazolo[l,5-6]pyridazines, while 3-hydrazinopyridazine 1-oxide gives 3-azidopyridazine 1-oxide (76TL3193, 76X725). 

Aldehyde enamines react with aromatic diazonium salts in two ways, depending on the degree of substitution at the enamine earbon (130). Thus the piperidine enamine of butyraldehyde (60) reacted with p-nitrophenyl-diazonium chloride to give the p-nitrophenylhydrazone of the a-keto aldehyde (190). 

The coupling of enamines with aromatic diazonium salts has been used for the syntheses of monoarylhydrazones of a-diketones (370,488-492) and a-ketoaldehydes (488,493). Cleavage of the initial enamine double bond and formation of the phenylhydrazone of acetone and acetophenone has been reported with the enamines of isobutyraldehyde and 2-phenylpropionalde-hyde. Rearrangement of the initial coupling product to the hydrazone tautomer is not possible in these examples. 

Almost all dyes are quinones or azaquinones of compound 2. The majority are used for thermal transfer processes a recent example is compound 306 (98USP5792587). The second major class are azo dyes, prepared either from aromatic diazonium salts as in compound 307 (95GEP4319296) or from a triazolopyridine 3-diazonium salt as in 308 (81BRP2054630). 

Aromatic diazonium salts are almost as important for reactions in which the diazonio group is lost as molecular nitrogen and in which aryl cations and radicals are the reagent proper (dediazoniation reactions, see Chs. 8 and 10). 

As explained in the preceding section, we will discuss the structure of aromatic diazonium salts on the basis of evidence from X-ray investigations. We will supplement those results with data obtained by other physical methods, in particular NMR and IR spectroscopy. Earlier experience with the more stable arenediazonium salts enabled those scientists who first obtained alkanediazonium ions in solution to characterize them by NMR spectroscopy (see Zollinger, 1995, Sec. 2.1). 

This summary of X-ray investigations of aromatic diazonium salts will concentrate on those results that are essential to understanding the structure and reactivity of these compounds. Most important are, first of all ... 

Aromatic diazonium salts react easily in neutral aqueous solution with thiols such as N-acetylcysteine, forming compounds of the type Ar — N2 —S —CH2CH(NHAc) COOH. Nifontov et al. (1990) suggested that such compounds, e.g., that of 5-diazo-imidazole-4-carboxylate, function as a form of transport depot for cytotoxic diazo-carboxylate in the human body. 

In the scientific sector, the understanding of the generally higher reactivity of heteroaromatic diazo components relative to that of aromatic diazonium salts has increased. The number of heterocyclic nitrogen atoms in azolediazonium ions has a marked influence on the N-H acidity of these ions. The pvalues of a series of such ions in aqueous solution at 0 °C (Scheme 12-4) indicate that the electrophilicity of the diazonio group in these compounds increases with the number of nitrogen atoms in the ring. ... 

The cycloaddition between furan and maleic anhydride was the first uncatalyzed aqueous Diels-Alder reaction reported in the literature and was studied by Diels and Alder themselves [11]. This cycloaddition was successfully revised by Woodward and Baer [12] and some years later by De Koning and coworkers [13]. The aqueous medium was also used in the cycloaddition of aromatic diazonium salts with methylsubstituted 1,3-butadienes [14]. 

Aromatic diazonium salts can, of course, be isolated (see Chapter 13), but only a few aliphatic diazonium salts have been prepared (see also Ref. 383). For reviews see Laali, K. Olah, G.A. Rev. Chem. Intermed., 1985, 6, 237 Bott, K. in Patai Rappoport The Chemistry of Functional Groups, Supplement C, pt. 1 Wiley NY, 1983, p. 671 Bott, K. Angew. Chem. Int. Ed. Engl., 1979, 18, 259. The simplest aliphatic diazonium ion CH3N2 has been prepared at — 120°C in superacid solution, where it lived long enough for an nmr spectrum to be taken Berner, D. McGarrity, J.F. J. Am. Chem. Soc., 1979, 101, 3135. 

Incidentally, 31 contributes more to the hybrid than 32, as shown by bond-distance measurements. In benzenediazonium chloride, the C—N distance is 1.42 A, and the N—N distance 1.08 A, which values lit more closely to a single and a triple bond than to two double bonds (see Table 1.5). Even aromatic diazonium salts are stable only at low temperatures, usually only below 5°C, though more stable ones, such as the diazonium salt obtained from sulfanilic acid, are stable up to 10 or 15°C. Diazonium salts are usually prepared in aqueous solution and used without isolation, though it is possible to prepare solid diazonium salts if desired (see 13-20). The stability of aryl diazonium salts can be increased by crown ether complexion. ... 

The decomposition of aromatic diazonium salts in neutral or alkaline solution generates radicals that attack supernatant benzene.64... 

Displacement of nitrogen from diazonium salts derived from 4- or 5-aminotriazoles can be achieved in the same manner as for other aromatic diazonium salts for example, diazotization of 4-amino-triazole-5-carboxamide and reaction with iodine and potassium iodide gives the 4-iodo derivative. ... 

The coupling of aromatic diazonium salts with a variety of aromatic compounds is the basis of the azo dye industry [2-5]. A variety of dying techniques are available but, fundamentally, two procedures are involved ... 

The reaction of phenacyltriphenylarsonium bromides (333) with aromatic diazonium salts in methanol containing sodium acetate provides a simple method for synthesizing 3,6-diaroyl-l,4-dihydro-l,2,4,5-tetrazines (334) in good yield (78JOM(155)293). The reaction has been postulated to proceed via the nitrilimine intermediate (335), whose formation can be explained by the sequence shown in Scheme 19. 

Triazenes have been prepared by the treatment of resin-bound aromatic diazonium salts with secondary amines (Figure 3.27). Regeneration of the amine can be effected by mild acidolysis (Entry 1, Table 3.23). Triazenes have been shown to be stable towards bases such as TBAF, potassium hydroxide, or potassium tert-butoxide [454], and under the conditions of the Heck reaction [455]. Primary amines cannot be linked to supports as triazenes because treatment of triazenes such as R-HN-N=N-Ar-Pol with acid leads to the release of aliphatic diazonium salts into solution [373]. Triazenes derived from primary amines can, however, be used for the preparation of amides and ureas (see Section 3.3.4),... 

Support-bound triazenes, which can be prepared from resin-bound secondary aliphatic amines and aromatic diazonium salts [455], undergo cleavage upon treatment with acids, leading to regeneration of the aromatic diazonium salts. In cross-linked polystyrene, these decompose to yield nitrogen and, preferentially, radical-derived products. If the acidolysis of polystyrene-bound triazenes is conducted in the presence of hydrogen-atom donors (e.g. THF), unsubstituted arenes can be obtained (Entries 8 and 9, Table 3.47). In the presence of alkenes or alkynes and Pd(OAc)2, the initially formed diazonium salts undergo Heck reaction to yield vinylated or alkynylated arenes (Entry 10, Table 3.47). Similarly, unsubstituted arenes can be obtained by oxida-... 

Few examples of the preparation of hydrazines or hydroxylamines on insoluble supports have been reported (Table 10.17). Hydrazines have been prepared by the reduction of aromatic diazonium salts or /V-nitroso amines (prepared from secondary amines by treatment with tert-butyl nitrite [340]), and by the N-amination of support-bound amines (Entry 3, Table 10.17). The direct reduction of hydrazones with borane to yield hydrazines on solid phase has not been reported, and appears to be difficult because of the ease with which the N-N bond of hydrazines is cleaved by reducing agents [340]. 

Cyclopentadiene triphenylarsorane (22) reacted with aromatic diazonium salts to give coupling products (24). 

The reaction of phenacyl or substituted-phenacyl triphenylarsonium bromide with aromatic diazonium salts gave l,4-dihydro-l,2,4,5-tetrazine (60) (6). 

Aromatic hydrazines are best prepared by reduction of aromatic diazonium salts (Table 23-4). 

The third mechanism of nucleophilic aromatic substitution, specific for substitution on aromatic diazonium salts, is shown in Equation 7.95. 

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