Hydrolysis ester synthesis

The action of esterases consists essentially in the hydrolysis (or synthesis) of carboxylic acid esters according to the equation ... 

Among the methods for preparing carboxylic acids carboxylation of a Grignard reagent and preparation and hydrolysis of a nitrile convert RBr to RCO2H The malonic ester synthesis converts RBr to RCH2CO2H... 

A number of specific Upases are used for ester synthesis (eq. 4) transesterification, eg, acidolysis with 1,3 specific Hpase (eq. 5) and hydrolysis reactions, eg, with nonspecific Hpase (eq. 6). 

The malonic ester synthesis can also be used to prepare cydoalkane-carboxvlic acids. For example, when 1,4-dibromobutanc is treated with diethyl malonate in the presence of 2 equivalents of sodium ethoxide base, the second alkylation step occurs intrcunotecidariy to yield a cyclic product. Hydrolysis and decarboxylation then give cvclopentanecarboxylic acid. Three-, four-, five-. 

Another alternative for preparing a primary amine from an alkyl halide is the Gabriel amine synthesis, which uses a phthalimide alkylation. An imide (—CONHCO—) is similar to a /3-keto ester in that the acidic N-H hydrogen is flanked by two carbonyl groups. Thus, imides are deprotonated by such bases as KOH, and the resultant anions are readily alkylated in a reaction similar to the acetoacetic ester synthesis (Section 22.7). Basic hydrolysis of the N-alkylated imide then yields a primary amine product. The imide hydrolysis step is analogous to the hydrolysis of an amide (Section 21.7). 

A more general method for preparation ofa-amino acids is the amidotnalmatesynthesis, a straightforward extension of the malonic ester synthesis (Section 22.7). The reaction begins with conversion of diethyl acetamidomalonate into an eno-late ion by treatment with base, followed by S 2 alkylation with a primary alkyl halide. Hydrolysis of both the amide protecting group and the esters occurs when the alkylated product is warmed with aqueous acid, and decarboxylation then takes place to vield an a-amino acid. For example aspartic acid can be prepared from, ethyl bromoacetate, BrCh CCHEt ... 

Acetoacetic ester synthesis (Section 22.7) The synthesis of a methyl ketone by alkylation of an alkyl halide, followed by hydrolysis and decarboxylation. 

Lipases can catalyze hydrolysis of esters, synthesis of esters, trans-esterification, and synthesis of some polymers. They have been applied in many fields including the food industry, fine chemistry, and the pharmaceutical industry. The low stability of native lipases makes them unsuitable for industrial applications. In order to use them more economically and efficiently, their operational stability can be improved by immobilization. Numerous efforts have been focused on the preparation of lipases in immobilized forms involving a variety of both support materials and immobilization methods [278],... 

The esters of nitrous acid are characterised by their high velocities of formation and hydrolysis. They are almost instantaneously decomposed by mineral acids and in the method of preparation given this has been taken into account. The slightest excess of hydrochloric acid must be avoided. Advantage is taken of this property of the alkyl nitrites in all cases where it is desired to liberate nitrous acid in organic solvents (in which metallic nitrites are insoluble). Examples addition of N203 to olefines, preparation of solid diazonium salts (p. 286), production of isonitroso-derivatives from ketones by the action of HN02. This synthesis is often also carried out in the manner of the acetoacetic ester synthesis, with ketone, alkyl nitrite, and sodium ethylate the sodium salt of the isonitrosoketone is formed (cf. in this connexion p. 259) ... 

The above-mentioned facts have important consequences on the stereochemical outcome of the kinetic resolution of asymmetrically substituted epoxides. In the majority of kinetic resolutions of esters (e.g. by ester hydrolysis and synthesis using lipases, esterases and proteases) the absolute configuration at the stereogenic centre(s) always remains the same throughout the reaction. In contrast, the enzymatic hydrolysis of epoxides may take place via attack on either carbon of the oxirane ring (Scheme 7) and it is the structure of the substrate and of the enzyme involved which determine the regioselec-tivity of the attack [53, 58-611. As a consequence, the absolute configuration of both the product and substrate from a kinetic resolution of a racemic... 

In most cases, the product of the malonic ester synthesis isn t the final product you re looking for. Commonly, the next step after the reaction in Figure 15-15 is hydrolysis and decarboxylation. Figure 15-16 shows this step. 

Lipases are enzymes that catalyze the in vivo hydrolysis of lipids such as triacylglycerols. Lipases are not used in biological systems for ester synthesis, presumably because the large amounts of water present preclude ester formation due to the law of mass action which favors hydrolysis. A different pathway (using the coenzyme A thioester of a carboxylic acid and the enzyme synthase [Blei and Odian, 2000]) is present in biological systems for ester formation. However, lipases do catalyze the in vitro esterification reaction and have been used to synthesize polyesters. The reaction between alcohols and carboxylic acids occurs in organic solvents where the absence of water favors esterification. However, water is a by-product and must be removed efficiently to maximize conversions and molecular weights. 

As mentioned above, in hydrolysis the ester may always be obtained with a high ee, but, what if the alcohol is required This problem may be eireumvented if the leaetion is inverted. Instead of hydrolysis, a synthesis may be performed, an esterification or better a transesterification in non-aqueous media (See Chapter 9). Sinee the enzyme shows the same stereopreferenee no matter the direetion of the reaetion (hydrolysis or transesterification), either the alcohol or the ester may be separated as the remaining substrate. If the ( -ester is the remaining substrate in hydrolysis the ( -alcohol will be the remaining substrate of transesterification (Figure 2.10). 

The dedd cells of the mycelium of Rhizopus arrhizus constitute d naturally immobilized lipdse very active in organic solvents. This immobilized enzyme was used for hydrolysis and synthesis of ester bonds triglycerides hydrolysis, and interesterification, esters and glycerides synthesis. More recently, the catalytic system has been applied in drug synthesis to the resolution of racemic esters with a good enantioselectivity. 

It is not possible to perform the acid hydrolysis without some ketonic hydrolysis occurring. This reaction and the preceding one are important in many syntheses of aliphatic ketones and acids. They might have been included equally well in the decomposition section (p. 411) in fact they are often referred to as the ketonic and acid decomposition of acetoacetic ester. The malonic ester synthesis of fatty acids may be compared with the present reaction (p. 135). 

The heart of the preparation of capsaicin is a malonic ester synthesis. The first step is bromination of the primary alcohol by phosphorous tribromide. The resulting primary alkyl bromide is used to alkylate the sodium salt of diethyl malonate. A substituted malonic acid derivative is obtained following basic hydrolysis of the ester groups. 

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