Hydrogenation dinitriles

Kinetic and thermodynamic aspects of THORPE ZIEGLER cyclization during the corirse of dinitriles hydrogenation will be discussed with all the by products. 

In the final step the dinitrile is formed from the anti-Markovrukov addition of hydrogen cyanide [74-90-8] at atmospheric pressure and 30—150°C in the hquid phase with a Ni(0) catalyst. The principal by-product, 2-methylglutaronitrile/4j5 j5 4-ti2-, when hydrogenated using a process similar to that for the conversion of ADN to hexamethylenediamine, produces 2-meth5i-l,5-pentanediamine or 2-methylpentamethylenediamine [15520-10-2] (MPMD), which is also used in the manufacture of polyamides as a comonomer. 

Its manufacture begins with the formation of dodecanedioic acid produced from the trimeri2ation of butadiene in a process identical to that used in the manufacture of nylon-6,12. The other starting material, 1,12-dodecanediamine, is prepared in a two-step process that first converts the dodecanedioic acid to a diamide, and then continues to dehydrate the diamide to the dinitrile. In the second step, the dinitrile is then hydrogenated to the diamine with hydrogen in the presence of a suitable catalyst. 

Hexamethylenediamine (HMDA), a monomer for the synthesis of polyamide-6,6, is produced by catalytic hydrogenation of adiponitrile. Three processes, each based on a different reactant, produce the latter coimnercially. The original Du Pont process, still used in a few plants, starts with adipic acid made from cyclohexane adipic acid then reacts with ammonia to yield the dinitrile. This process has been replaced in many plants by the catalytic hydrocyanation of butadiene. A third route to adiponitrile is the electrolytic dimerization of acrylonitrile, the latter produced by the ammoxidation of propene. 

Many hydrogenation and polymerization reactions in the chemical industry are carried out with liquid-phase reactants. An example is the hydrogenation of aliphatic dinitriles to produce diamines (108,109), which are subsequently converted with adipic acid in solution and polymerized to produce linear polyamides, including nylon 6,6. Recently, the development of wet-environmental transmission electron microscopy (wet-ETEM) for direct nanoscale probing of... 

Trimethoprim has also been synthesized by condensing 3,4,5-trimethoxybenzaldehyde with malonic acid dinitrile in a Knoevenagel reaction, which forms the derivative (33.1.53), which is partially reduced to the enamine (33.1.54) by hydrogen using a palladium on carbon catalyst, which upon being reacted with guanidine is transformed into trimethoprim [52,53]. 

Preparative routes to 5/7-dibenz[6,e]azepine-6,11 -diones (morphanthridinediones) are based mainly on the cyclization of 2-aminobenzophenone-2 -carboxylic acids and their derivatives (55LA(594)89). Studies on a-aminodiphenyImethane-2 -carboxylic acid reveal that cyclization to 5,11 -dibenz[6,e ]azepinone (188) is much slower at room temperature than the cyclizations of the analogous 2-aminobiphenyl-2 -carboxylic acid and the 2 -aminobiphenylacetic acid (189), which at room temperature cyclize spontaneously to phenanthridone and dibenz[f>,d]azepin-6-one (190) respectively (61JOC1329). The hydrogen bromide-induced cyclization of dinitriles (Scheme 16) is adaptable to the synthesis of 2-amino-7-bromo-3//-azepines and 5H-dibenz[c,e]azepin-7-ones (67JOC3325). Apparently, for unsymmetrical dinitriles cyclization is such as always to give the azepine with the bromo substituent attached to the carbon of the a,j8-unsaturated nitrile as exemplified in Scheme 16. 

Problem 18.47 What is the product of catalytic hydrogenation of (a) acetone oxime, b) propane-1,3-dinitrile, (c) propanal and methylamine M... 

FBR commonly applied in petrochemicals and bioprocesses, it only has few applications in hydrogenations phenylacetylene, dinitriles. 

In the course of the catalytic hydrogenation of a,us dinitriles over Raney nickel, by-products are obtained from C-N and C-C bond formation. The mechanism of the formation of these compounds was investigated. Cyclic and linear secondary amines can result from the same secondary imine through a transimination process involving a ring-chain tautomerism. Stereochemical results for 2-aminomethyl-cyclopentylamine (AMCPA) are in accordance with a specific cyclisation pathway favored by an intramolecular hydrogen bond giving rise to the cis isomer from aminocapro-nitrile, unfavored in the case of adiponitrile which leads to the trans AMCPA as the major isomer. 

We have investigated the catalytic hydrogenation of a,us di-cyanoalkanes and we report results with 1,4-dicyanobutane (ADN). Scheme 1 details the intermediates involved in a step-by-step addition of hydrogen to the dinitrile molecule adsorbed on the metal surface. Some of them are to be considered as precursors for the formation of by-products (detected in the liquid phase after desorption). 

This preparation illustrates the alkylation of malononitrile under acid-catalyzed conditions, and the use of diborane for the reduction of a dinitrile to a diamine. The procedure for the preparation of tert-butylmalononitrile has been outlined briefly by Boldt and co-workers.2 The generation of diborane in situ and the general method for nitrile reduction is that described by Brown and co-workers.3 Attempts to reduce the dinitrile to the diamine by other methods including catalytic hydrogenation (5% rhodium on alumina, 5 atm.), lithium aluminum hydride, and lithium aluminum hydride-aluminum chloride were singularly unsuccessful. 

Fumaric and maleic dinitriles react similarly, but the 4,5-dicyanotriazolines formed in situ lose a molecule of hydrogen cyanide and give a triazole with the... 

In the simplest case, reaction of a primary monoamine via a two-fold Michael reaction with acrylonitrile (bis-cyanoethylation) led to the dinitrile (Fig. 1.1). Subsequent reduction of the two nitrile functions - by hydrogenation with sodium borohydride in the presence of cobalt(II) ions - afforded the corresponding terminal diamine. Repetition (iteration) of this synthetic sequence, consisting in Michael addition followed by reduction, provided the first - structurally variable - access to regularly branched, many-armed molecules. 

Ring hydrogens on highly substituted aryl selenopyrans can be selectively replaced by bromination or nitration. Halo substituents on the selenopyrans can be readily displaced using copper cyanide affording the mono- and dinitrile derivatives (Scheme 3) <2002J(P2)1909>. 

The cyclization reactions of a,oj-dinitriles under the influence of anhydrous hydrogen halides (Eq. 3) at 0-25° have proved to be of considerable synthetic value. A range of aromatic heterocyclic systems becomes available, since it is possible for the exo-imine double... 

A few early references ascribe cyclic structures to the action of hydrogen halides on a, j-dinitriles. Soderback89 assigned structure... 

The action of hydrogen chloride on adiponitrile has been the subject of an extensive study by Zil berman and his associates. Much of the work has been reviewed.99 No cyclic compounds were observed with this dinitrile or its j8-methyl homolog. The action of other halogen acids on adiponitriles has not been investigated. Higher aliphatic a,cu-dinitriles have received no attention. 

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