Organic acid anhydride

The nomenclature of organic acid anhydrides is derived from the names of the constituent carboxylic acids. In symmetrical acid anhydrides, only the prefix of the original carboxylic acid is used and the suffix "anhydride" is added. For most unsymmetrical acid anhydrides - also called mixed anhydrides- the prefixes from both acids reacted are listed before the suffix, e.g., benzoic propanoic anhydride. ==Preparation==

Organic acid anhydrides are prepared in industry by diverse means. Acetic anhydride is mainly produced by the carbonylation of methyl acetate. Maleic anhydride is produced by the oxidation of benzene or butane. Laboratory routes emphasize the dehydration of the corresponding acids. The conditions vary from acid to acid, but acetic anhydride (itself an acid anhydride) is a common dehydrating agent as illustrated by the preparation of 3-nitrophthalic anhydride: : In addition to symmetrical, acyclic anhydrides, other classes are recognized as discussed in the following sections. Mixed anhydrides Mixed anhydrides have the formula RC(O)OC(O)R'. They tend to redistribute upon heating although acetic formic anhydride can be distilled at one atmosphere. :CH3C(O)Cl + HCO2Na → HCO2COCH3 + NaCl Cyclic anhydrides Cyclic anhydrides, a kind of a heterocycle, are derived from some dicarboxylic acids. Commercially important examples are those that form five- and six-membered rings, succinic anhydride, maleic anhydride, and phthalic anhydride. Although these five-membered rings form readily, they can be opened. Cyclic anhydrides with smaller rings are only of academic interest, e.g., malonic anhydride. Cyclic anhydrides that would give larger rings, e.g. from adipic acid, are no importance. Dianhydrides and trianhydrides The following examples are mostly cyclic anhydrides: • 1,2,3,4-butanetetracarboxylic dianhydride produced by dehydration of 1,2,3,4-butanetetracarboxylic acid. • naphthalenetetracarboxylic dianhydride • 1,2,4,5-Benzenetetracarboxylic dianhydride and 1,2,3,4-Benzenetetracarboxylic dianhydride • Mellitic anhydride, a trianhydride These compounds are sometimes useful crosslinking agents. ==Reactions==

Acid anhydrides are a source of reactive acyl groups, and their reactions and uses resemble those of acyl halides. For example, they are useful in Friedel-Crafts acylation of arenes (ArH): : Unlike acid halides, however, anhydrides do not react with Gilman reagents. Acid anhydrides tend to be less electrophilic than acyl chlorides. Usually only one acyl group is transferred per molecule of acid anhydride, which generall leads to a lower atom efficiency. The low cost, however, of acetic anhydride makes it a common choice for acetylation reactions. Acylations with cyclic anhydrides can be distinctive vs the acyclic anhydrides, e.g. for the preparation of keto acids. The action of phthalic anhydride on the electron-rich phenols results in diacylation. In reactions with alcohols and amines, the reactions afford equal amounts of the acylated product and the carboxylic acid: : : The reactivity of anhydrides can be enhanced by using a catalytic amount of N,N-dimethylaminopyridine ("DMAP") or even pyridine. First, DMAP (2) attacks the anhydride (1) to form a tetrahedral intermediate, which collapses to eliminate a carboxylate ion to give amide 3. This intermediate amide is more activated towards nucleophilic attack than the original anhydride, because dimethylaminopyridine is a better leaving group than a carboxylate. In the final set of steps, a nucleophile (Nuc) attacks 3 to give another tetrahedral intermediate. When this intermediate collapses to give the product 4, the pyridine group is eliminated and its aromaticity is restored – a powerful driving force, and the reason why the pyridine compound is a better leaving group than a carboxylate ion. For prochiral cyclic anhydrides, the alcoholysis reaction can be conducted asymmetrically. ==Applications and occurrence of acid anhydrides==

File:Acetic anhydride2DACS.svg|Acetic anhydride is produced on a large scale for many applications. File:Naphthalenetetracarboxylic dianhydride.svg|Naphthalenetetracarboxylic dianhydride, a building block for complex organic compounds, is an example of a dianhydride. File:Maleic anhydride (vertical).svg|Maleic anhydride is a cyclic anhydride, widely used to make industrial coatings. File:Adenosintriphosphat protoniert.svg|ATP in its protonated form is an anhydride derived from phosphoric acid. File:1,3-Bisphosphoglyceric acid.svg|The "mixed anhydride" 1,3-bisphosphoglyceric acid occurs widely in metabolic pathways. File:3'-Phosphoadenosine-5'-phosphosulfate.svg|3'-Phosphoadenosine-5'-phosphosulfate (PAPS) is a mixed anhydride of sulfuric and phosphoric acids and is the most common coenzyme in biological sulfate transfer reactions. Acetic anhydride is a major industrial chemical widely used for preparing acetate esters, e.g. cellulose acetate. Maleic anhydride is the precursor to various resins by copolymerization with styrene. Maleic anhydride is a dienophile in the Diels-Alder reaction. Dianhydrides, molecules containing two acid anhydride functions, are used to synthesize polyimides and sometimes polyesters and polyamides. Examples of dianhydrides: pyromellitic dianhydride (PMDA), 3,3', 4,4' - oxydiphtalic dianhydride (ODPA), 3,3', 4,4'-benzophenone tetracarboxylic dianhydride (BTDA), 4,4'-diphtalic (hexafluoroisopropylidene) anhydride (6FDA), benzoquinonetetracarboxylic dianhydride, ethylenetetracarboxylic dianhydride. Polyanhydrides are a class of polymers characterized by anhydride bonds that connect repeat units of the polymer backbone chain. Biological occurrence Natural products containing acid anhydrides have been isolated from animals, bacteria and fungi. Examples include cantharidin from species of blister beetle, including the Spanish fly, Lytta vesicatoria, and tautomycin, from the bacterium Streptomyces spiroverticillatus. The maleidride family of fungal secondary metabolites, which possess a wide range of antibiotic and antifungal activity, are alicyclic compounds with maleic anhydride functional groups. A number of proteins in prokaryotes and eukaryotes undergo spontaneous cleavage between the amino acid residues aspartic acid and proline via an acid anhydride intermediate. In some cases, the anhydride may then react with nucleophiles of other cellular components, such as at the surface of the bacterium Neisseria meningitidis or on proteins localized nearby. ==Analogues==

Nitrogen Imides are structurally related analogues, where the bridging oxygen is replaced by nitrogen. They are similarly formed by the condensation of dicarboxylic acids with ammonia. The replacement of all oxygen atoms with nitrogen gives imidines, these are a rare functional group which are very prone to hydrolysis. Sulfur Sulfur can replace oxygen, either in the carbonyl group or in the bridge. In the former case, the name of the acyl group is enclosed in parentheses to avoid ambiguity in the name, e.g., (thioacetic) anhydride (CH3C(S)OC(S)CH3). When two acyl groups are attached to the same sulfur atom, the resulting compound is called a thioanhydride, e.g., acetic thioanhydride ((CH3C(O))2S). ==See also==