Acid anhydride
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An acid anhydride is an organic compound that has two acyl groups bound to the same oxygen atom.[1] Most commonly, the acyl groups are derived from the same carboxylic acid, the formula of the anhydride being (RC(O))2O. Symmetrical acid anhydrides of this type are named by replacing the word acid in the name of the parent carboxylic acid by the word anhydride.[2] Thus, (CH3C(O))22O is called acetic anhydride. Mixed (or unsymmetrical) acid anhydrides, such as acetic formic anhydride (see below), are known.
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[edit] Important acid anhydrides
Acetic anhydride is a major industrial chemical widely used for preparing acetate esters. The cyclic acid anhydride maleic anhydride is used in organic synthesis as dienophile in the Diels-Alder reaction. One or both acyl groups of an acid anhydride may also be derived from a sulfonic acid or a phosphonic acid. The mixed anhydride 1,3-bisphosphoglycerate is an intermediate in the formation of ATP via glycolysis.[3]
[edit] Preparation
Acid anhydrides are prepared in industry by diverse means. Acetic anhydride is mainly produced by the carbonylation of methyl acetate.[4] Maleic anhydride is produced by the oxidation of butane. For pedogical and practical considerations, laboratory routes emphasize the dehydration of the corresponding acids. The conditions vary from acid to acid, but phosphorus pentoxide is a common dehydrating agent:
- 2 CH3COOH + P4O10 → CH3C(O)OC(O)CH3 + "(HO)2P4O9"
Acid chlorides are also effective precursors:[5]
- CH3C(O)Cl + HCO2Na → HCO2COCH3 + NaCl
[edit] Reactions
Acid anhydrides are a source of reactive acyl groups, and their reactions and uses resemble those of acyl halides. In reactions with protic substrates, the reactions afford equal amounts of the acylated product and the carboxylic acid:
- RC(O)OC(O)R + HY → RC(O)Y + RCO2H
for HY = H2O, HOR (alcohols), HNR'2 (ammonia, primary, secondary amines), aromatic ring (see Friedel-Crafts acylation).
Acid anhydrides tend to be less electrophilic than acyl chlorides, and only one acyl group is transferred per molecule of acid anhydride, which leads to a lower atom efficiency. The low cost, however, of acetic anhydride makes it a common choice for acetylation reactions. Furthermore, the avoidance of chlorocarbons is preferred from the environmental perspective.
[edit] Sulfur analogues
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,[2] 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,[2] e.g., acetic thioanhydride ((CH3C(O))2S).
[edit] References
- ^ International Union of Pure and Applied Chemistry. "acid anhydrides". Compendium of Chemical Terminology Internet edition.
- ^ a b c International Union of Pure and Applied Chemistry (1993). "Recommendation R-5.7.7." A Guide to IUPAC Nomenclature of Organic Compounds. Oxford: Blackwell Science. ISBN 0-632-03488-2. pp. 123–25.
- ^ Nelson, D. L.; Cox, M. M. "Lehninger, Principles of Biochemistry" 3rd Ed. Worth Publishing: New York, 2000. ISBN 1-57259-153-6.
- ^ Zoeller, J. R.; Agreda, V. H.; Cook, S. L.; Lafferty, N. L.; Polichnowski, S. W.; Pond, D. M. "Eastman Chemical Company Acetic Anhydride Process" Catalysis Today (1992), volume 13, pp.73-91. doi:10.1016/0920-5861(92)80188-S
- ^ Lewis I. Krimen (1988). "Acetic Formic Anhydride". Org. Synth.; Coll. Vol. 6: 8.
