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Aminophenol catalysts

Resorcinol Derivatives. Aminophenols (qv) are important intermediates for the syntheses of dyes or active molecules for agrochemistry and pharmacy. Syntheses have been described involving resorcinol reacting with amines (91). For these reactions, a number of catalysts have been used / -toluene sulfonic acid (92), zinc chloride (93), zeoHtes and clays (94), and oxides supported on siUca (95). In particular, catalysts performing the condensation of ammonia with resorcinol have been described gadolinium oxide on siUca (96), nickel, or zinc phosphates (97), and iron phosphate (98). [Pg.491]

Condensation Reactions. Condensation of substituted ben2aldehydes with 2-aminophenol in the presence of a catalyst (aluminum, iron,... [Pg.310]

Aminophenols are either made by reduction of nitrophenols or by substitution. Reduction is accompHshed with iron or hydrogen in the presence of a catalyst. Catalytic reduction is the method of choice for the production of 2- and 4-aminophenol (see Amines BY reduction). Electrolytic reduction is also under industrial consideration and substitution reactions provide the major source of 3-aminophenol. [Pg.310]

In another process variant, only 88% of the nitrobenzene is reduced, and the reaction mixture then consists of two phases the precious metal catalyst (palladium on activated carbon) remains in the unreacted nitrobenzene phase. Therefore, phase separation is sufficient as work-up, and the nitrobenzene phase can be recycled direcdy to the next batch. The aqueous sulfuric acid phase contains 4-aminophenol and by-product aniline. After neutralization, the aniline is stripped, and the aminophenol is obtained by crystallization after the aqueous phase is purified with activated carbon (53). [Pg.311]

In an alternative industrial process, resorcinol [108-46-3] is autoclaved with ammonia for 2—6 h at 200—230°C under a pressurized nitrogen atmosphere, 2.2—3.5 MPa (22—35 atm). Diammonium phosphate, ammonium molybdate, ammonium sulfite, or arsenic pentoxide maybe used as a catalyst to give yields of 60—94% with 85—90% selectivity for 3-aminophenol (67,68). A vapor-phase system operating at 320°C using a siUcon dioxide catalyst impregnated with gallium sesquioxide gives a 26—31% conversion of resorcinol with a 96—99% selectivity for 3-aminophenol (69). [Pg.311]

BMI—y -aminophenol adducts can further react with epoxy resia and subsequendy be cured with imida2ole catalyst. 1 2 BMI—aminophenol adducts have been used as curing agents for epoxy resia (37). [Pg.27]

Heat-resistant resin compositions based on bismaleknide—epoxy blends are achieved by reaction of a BMI—y -aminophenol [591-27-5] (1 1) adduct with epoxy. This prepolymer is fully cured with an imida2ole catalyst (54). Blends of hydroxy-terminated BMI—aminophenol adducts can easily be B-staged, that is, prepolymerked, and subsequendy ground to provide a powder that can be molded by the appHcation of heat and pressure. [Pg.30]

A direct catalytic conversion of esters, lactones, and carboxylic acids to oxazolines was efficiently achieved by treatment with amino alcohols in the presence of the tetranuclear zinc cluster Zn4(0C0CF3)60 as catalyst, essential for condensation and cyclodehydration reactions. For example, the use of (5)-valinol allowed the easy synthesis of oxazolines 125 and 126 in satisfactory yields <06CC2711>. A one-pot direct preparation of various 2-substituted oxazolines (as well as benzoxazoles and oxadiazoles) was also performed from carboxylic acids and amino alcohols (or aminophenols or benzhydrazide) using Deoxo-Fluor reagent <06TL6497>. [Pg.303]

The Akiyama group tested various BINOL phosphates 3 as catalysts for the indirect Mannich reaction of aldimines 8 derived from 2-aminophenol with silyl ketene acetals 9 (Scheme 4). All of these Brpnsted acids furnished P-amino ester 10a in (nearly) quantitative yields. Both the reaction rates (4-46 h) and the enantioselectivities (27-87% ee) were strongly dependent on the nature of the substituents at the 3,3 -positions. [Pg.400]

Eichhom and his co-workers have thoroughly studied the kinetics of the formation and hydrolysis of polydentate Schiff bases in the presence of various cations (9, 10, 25). The reactions are complicated by a factor not found in the absence of metal ions, i.e, the formation of metal chelate complexes stabilizes the Schiff bases thermodynamically but this factor is determined by, and varies with, the central metal ion involved. In the case of bis(2-thiophenyl)-ethylenediamine, both copper (II) and nickel(II) catalyze the hydrolytic decomposition via complex formation. The nickel (I I) is the more effective catalyst from the viewpoint of the actual rate constants. However, it requires an activation energy cf 12.5 kcal., while the corresponding reaction in the copper(II) case requires only 11.3 kcal. The values for the entropies of activation were found to be —30.0 e.u. for the nickel(II) system and — 34.7 e.u. for the copper(II) system. Studies of the rate of formation of the Schiff bases and their metal complexes (25) showed that prior coordination of one of the reactants slowed down the rate of formation of the Schiff base when the other reactant was added. Although copper (more than nickel) favored the production of the Schiff bases from the viewpoint of the thermodynamics of the overall reaction, the formation reactions were slower with copper than with nickel. The rate of hydrolysis of Schiff bases with or/Zw-aminophenols is so fast that the corresponding metal complexes cannot be isolated from solutions containing water (4). [Pg.162]

An interesting approach to maleimide-terminated phenoxy resin has recently has described (42). para-Maleimidobenzoic acid was reacted with diglyci-dylbisphenol-A epoxy resin in the presence of catalyst to provide the bismale-imide of Fig. 13. Instead of diglycidyl bisphenol-A, linear epoxy resin pre-polymers can be used in this reaction to form a maleimide terminated phenoxy resin. Another suitable functionalized monomaleimide is m- or p- N-(hydroxyphenyl) maleimide which is synthesized from maleic anhydride and m-aminophenol in DMF as a solvent at 70 °C. The purified hydroxyphenyl maleimide was reacted with epoxy resin to form novel BMIs as outlined in Fig. 14. The new BMI and phenoxy oligomers polymerize at temperatures of 200-220 °C, but the cure temperatures can be significantly lowered when catalysts such as imidazoles or triphenylphosphine are added. The cured homopolymers show Tg of 140 and 230 °C for the n = 2 and the n = 1 polymer, respectively(43). [Pg.180]

Heat resistant resin compositions based on BMI/aminophenol-Epoxy blends are achieved by reacting a BMI/p-aminophenol 1 1 adduct with epoxy resin (62). Both the secondary amine and phenol functionality may react with the epoxy resin and subsequently cure through an imidazole catalyst. Imidazole catalysts promote both the epoxy/phenol reaction and the anionic maleimide crosslinking. The formation of a 1 2 BMI/aminophenol adduct, as in Fig. 20, is claimed in a patent (63). The hydroxy terminated BMI/aminophenol adduct is an advantageous curing agent for epoxy resins when high temperature performance is desired. [Pg.188]

Traditional routes to phenoxazines include the thermolysis of 2-aminophenol and catechol, the latter acting as an acid catalyst, or catechol and ammonia. Phenothiazines are prepared similarly by heating diphenylamines with sulfur (Scheme 10) (B-78MI22701). 2-Hydroxy- (or mercapto-) 2, 4 -dini-trodiphenylamines cyclize to phenoxazines (or phenothiazines) in base by elimination of nitrous acid. This reaction is complicated by Smiles-type rearrangement so that mixtures of isomeric products are obtained (Scheme 11). [Pg.663]

Traditional routes to phenoxazines include the thermolysis of 2-aminophenol and catechol, the latter acting as an acid catalyst, or catechol and ammonia. Phenothiazines are prepared similarly by heating diphenylamines with sulfur (Scheme 111). [Pg.1033]

Paracetamol - [AMINOPHENOLS](Vol2) -platinum-group metals catalyst for [PLATINUM-GROUP METALS] (Vol 19)... [Pg.722]

In 1997, the first truly catalytic enantioselective Mannich reactions of imines with silicon enolates using a novel zirconium catalyst was reported [9, 10]. To solve the above problems, various metal salts were first screened in achiral reactions of imines with silylated nucleophiles, and then, a chiral Lewis acid based on Zr(IV) was designed. On the other hand, as for the problem of the conformation of the imine-Lewis acid complex, utilization of a bidentate chelation was planned imines prepared from 2-aminophenol were used [(Eq. (1)]. This moiety was readily removed after reactions under oxidative conditions. Imines derived from heterocyclic aldehydes worked well in this reaction, and good to high yields and enantiomeric excesses were attained. As for aliphatic aldehydes, similarly high levels of enantiomeric excesses were also obtained by using the imines prepared from the aldehydes and 2-amino-3-methylphenol. The present Mannich reactions were applied to the synthesis of chiral (3-amino alcohols from a-alkoxy enolates and imines [11], and anti-cc-methyl-p-amino acid derivatives from propionate enolates and imines [12] via diastereo- and enantioselective processes [(Eq. (2)]. Moreover, this catalyst system can be utilized in Mannich reactions using hydrazone derivatives [13] [(Eq. (3)] as well as the aza-Diels-Alder reaction [14-16], Strecker reaction [17-19], allylation of imines [20], etc. [Pg.144]

Aromatic and heterocyclic nitro compounds are readily reduced in good yield to the corresponding amines (e.g. o-aminophenol, Expt 6.50) by sodium borohydride in aqueous methanol solution in the presence of a palladium-on-carbon catalyst. In this reduction there is no evidence for the formation of intermediates of the azoxybenzene or azobenzene type, although if the reaction is carried out in a polar aprotic solvent, such as dimethyl sulphoxide, azoxy compounds may sometimes be isolated as the initial products. [Pg.891]

Co-product and by-product AS production depends on the process that is used to make the primary product - as shown in Table 12.3. Small amounts of AS may also be recovered in other processes such as acrylonitrile, acrylamide, formic acid, hydrogen cyanide, hydroquinone and p-aminophenol, and from the neutralization of sulfuric acid used to make clays and catalysts for catalytic cracking242. [Pg.293]

Similar carbonylations of 220 in the presence of o-aminophenols 223, facilitated with a Cu(I) co-catalyst, afford the benzanilide derivatives 224,... [Pg.264]

By investigating the influence of the acid strength of various proton donor catalysts on the kinetics of the reaction, Antoni8 showed that the reaction rate increases with decreasing pK . This explained why several authors7,9 10 had obtained better yields with o-aminophenol hydrochloride (pK 4.5) than with catechol (pK 9.9) however the yield of phenoxazine did not exceed 30%. [Pg.85]

Although the earliest examples of the use of US as a substitute for phase transfer catalysts in organic addition reactions were reported more than two decades ago and a number of such reactions have since been improved as a result [1-7], the sole analytical application exploiting this potential is a method for the determination of paracetamol where the drug is derivatized by hydrolysis to p-aminophenol, which reacts with o-cresol in an alkaline medium to form the Indophenol Blue dye, according to the following reaction ... [Pg.231]


See other pages where Aminophenol catalysts is mentioned: [Pg.310]    [Pg.51]    [Pg.192]    [Pg.195]    [Pg.95]    [Pg.118]    [Pg.453]    [Pg.80]    [Pg.87]    [Pg.22]    [Pg.563]    [Pg.417]    [Pg.404]    [Pg.177]    [Pg.362]    [Pg.155]    [Pg.292]    [Pg.472]    [Pg.362]    [Pg.588]    [Pg.122]    [Pg.118]    [Pg.5763]    [Pg.35]   
See also in sourсe #XX -- [ Pg.472 , Pg.477 ]




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Aminophenols

Imidazoline-aminophenol nickel catalyst

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