Diazotation

It is prepared by an intramolecular transformation of diazoaminobenzene in the presence of aniline hydrochloride, or in one stage by diazotizing a solution of aniline and aniline hydrochloride with an insufficient amount of nitrous acid. 

Prepared by reduction of 4-nitrophenol or 4-nitrosophenoi. Can be diazotized and used as a first component in azo-dyes. Chief outlet is for sulphur dyes in which it is fused with sodium polysulphides. L/sed as a photographic developer. 

It is an important dyestuffs intermediate. It condenses with chloroethanoic acid to give phenylglycine-o-carboxylic acid for the synthesis of indigo. It can be diazotized and used as a first component in azo-dyes it condenses also with chloroanthraquinones to give intermediates for anthraquinone dyes. 

M.p. 127 5°C. Dibasic, readily diazotizes. Prepared by treating hydrazobenzene with hydrochloric acid, intramolecular rearrangement taking place. 

Other chlorinated naphthalenes. The other monochloronaphthalene (2-), the ten theoretically possible dichloronaphthalenes, and the fourteen trichloronaphthalenes have all been prepared, generally from the corresponding amino-derivatives by diazotization and treatment with CuCl. They are of little industrial importance. 

The most important reaction of the diazonium salts is the condensation with phenols or aromatic amines to form the intensely coloured azo compounds. The phenol or amine is called the secondary component, and the process of coupling with a diazonium salt is the basis of manufacture of all the azo dyestuffs. The entering azo group goes into the p-position of the benzene ring if this is free, otherwise it takes up the o-position, e.g. diazotized aniline coupled with phenol gives benzeneazophenol. When only half a molecular proportion of nitrous acid is used in the diazotization of an aromatic amine a diazo-amino compound is formed. 

I-Naphthylamine readily diazotizes and couples to aromatic hydroxylic or basic compounds. It was thus used as a first component in a number of important monoazo dyes, but its use has been severely curtailed because of its potent carcinogenicity. It sulphonates to give naphthionic acid (l-naphthylamine-4-sul-phonic acid). 

Ditrosonium hydrogen sulphate, chamber crystals, NOHSO4. White solid m.p. 73°C (decomp.). Prepared SO2 and fuming nitric acid. Used in diazotization. 

Basic, forms a stable water-soluble dihydrochloride. Diazotization gives brown azodyes (Bismarck brown) owing to the coupling of the partially diazotized base with the excess of diamine. Is also used as an end component of many azo-dyes, readily coupling with one or two molecules of diazo compound. 

CgHgNa. While crystals m.p. 147 C, b.p. 267"C, darken rapidly in air. Prepared by reducing p-nitroaniline or aminoazobenzene. Oxidizing agents convert it to quinone derivatives, hence it cannot be diazotized with nitric acid. 

C HgNjOjS. Colourless needles, with iH20. Prepared by reducing diazotized sulphanilic acid with an excess of sodium sulphite. It is a typical hydrazine in its reactions with ketones, and with acetoacetic ester. The latter reaction gives rise to the tartrazine dyestuffs, and is much used commercially. 

It is prepared by heating aniline sulphate for 8 hours at l C. It readily diazotizes and is used as first component in a large variety of azo dyes. 

When an aqueous solution of a diazonium salt is added to an alkaline solution of a phenol, coupling occurs with formation of an azo-compound (p. 188). If ho vc cr the ntiueous solution of the diazonium salt, t. . ., />-bromohenzene diazonium chloride, is mixed with an excess of an aromatic hydrocarbon, and aqueous sodium hydroxide then added to the vigorously stirred mixture, the diazotate which is formed, e.g., BrC,H N OH, dissolves in the hydrocarbon and there undergoes decomposition with the formation of nitrogen and two free radicals. The aryl free radical then reacts with the hydrocarbon to give a... 

The free radical mechanism is confirmed by the fact that if a substituted aromatic hydrocarbon is used in this reaction, the incoming group (derived from the diazotate) may not necessarily occupy the position in the benzene ring normally determined by the substituent present—a characteristic of free radical reactions. 

The diazonium salts 145 are another source of arylpalladium com-plexes[114]. They are the most reactive source of arylpalladium species and the reaction can be carried out at room temperature. In addition, they can be used for alkene insertion in the absence of a phosphine ligand using Pd2(dba)3 as a catalyst. This reaction consists of the indirect substitution reaction of an aromatic nitro group with an alkene. The use of diazonium salts is more convenient and synthetically useful than the use of aryl halides, because many aryl halides are prepared from diazonium salts. Diazotization of the aniline derivative 146 in aqueous solution and subsequent insertion of acrylate catalyzed by Pd(OAc)2 by the addition of MeOH are carried out as a one-pot reaction, affording the cinnamate 147 in good yield[115]. The A-nitroso-jV-arylacetamide 148 is prepared from acetanilides and used as another precursor of arylpalladium intermediate. It is more reactive than aryl iodides and bromides and reacts with alkenes at 40 °C without addition of a phosphine ligandfl 16]. 

Butler recently reviewed the diazotization of heterocyclic amines (317). Reactions with nitrous acid yield in most cases N-exocyclic compounds. Since tertiary amines are usually regarded as inen to nitrosation, this... 

The weakly basic 2-aminothiazoles are most readily diazotized in concentrated solutions of oxygen containing acids such as sulfuric acid, 40 to 50% (322-326) fiuoroboric phosphoric acids (589) phosphoric acid (327, 328) and mixtures of phosphoric and nitric acid (74. 322, 323. 329-331). From strong acid solutions, solid diazonium salts can be isolated (34, 332. 333). 

Methyl-5-aminothia2ole-4-carboxylic acid is diazotized with isoamyl nitrite in the presence of furan in 1.2-dichloroethane to give a mixture of products 163 (53%), 164 (33%). 165 (11%), and 166 (3%) (Scheme 104) (334). This reactivity experiment was carried out to examine the possibility of the occurrence of 4,5-dehydrothiazole (hetaryne). Hetaryne intermediates seem not to be involved as an intermediate in the reaction. The formation of 163 through 166 can be rationalized in terms of the intermediacy of 166a. 

When carried out in dilute acid, diazotization of 2-aminothia2ole may provide unstable diazohydroxides (164, 335, 336), differing in that respect from 2-aminopyridines which give 2-pyridones when the reaction is carried out in weak acids (337). 

Even when deactivated by nitro substitution on C-5, the 2-aminothiazoles still undergo diazotization (35, 338-340). As with carbonyl derivatives (Section III.2.B), competition may occur between N nucleophilic reactivity and nitrosation of the 5-position when it is unsubstituted (341-344). 

Some recent general reviews deal with the mechanism of N-nitrosation in aqueous solution (345), the nitrosation of secondary amines (346). the effect of solvent acidity On diazotization (347) and the reactivity of diazonium salts (1691). Therefore, a complete rationalization of the reactivity of amino azaaromatics would be timelv. 

Yields can be very good Beyer (402) reports a 90% yield when coupling 2-amino-4-phenylthiazole with the diazonium salt of aniline. The coupling of diazotized anilines under modified conditions has been reported in a work treating the preparation of antineoplastics (403). 

Amino-5-methylthiazole does not react with diazotized p-nitroaniline in solutions acidified with acetic or hydrochloric acid (391). 2-Amino-4,5-dimethylthiazole with the diazonium salts of para-substituted anilines, however, gives product 193, involving reactivity of the exocyclic nitrogen (Scheme 122) (399). 

Diazonium salts of thiazoles are among the most widely used intermediates in thiazole chemistry. They are prepared by diazotization of... 

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