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Acetic oxalic anhydride

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Acetic oxalic anhydride
Ball-and-stick model of the acetic oxalic anhydride molecule
Names
Preferred IUPAC name Diacetic oxalic dianhydride
Other names Diacetyl oxalate
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H6O6/c1-3(7)11-5(9)6(10)12-4(2)8/h1-2H3Key: XRMBFFGBVGXJJF-UHFFFAOYSA-N
SMILES
  • CC(OC(C(OC(C)=O)=O)=O)=O
Properties
Chemical formula C6H6O6
Molar mass 174.108 g·mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkY verify (what is  ?) Infobox references
Chemical compound

Acetic oxalic anhydride is an organic compound with a chemical formula of C
6H
6O
6 and a structural formula of (H3C-(C=O)-O-(C=O)-)2. It can be viewed as a mixed anhydride, formally derived from acetic acid (H3C-(C=O)OH) and oxalic acid ((-(C=O)OH)2), in 2:1 molecular ratio, by the loss of two water molecules.

Preparation

Unlike some other anhydrides, Acetic oxalic anhydride cannot be obtained directly from the acids. It was synthesized in 1953 by W. Edwards and W. M. Henley, by reacting silver oxalate (Ag
2C
2O
4) suspended in diethyl ether with acetyl chloride at temperatures below −5 °C and distilling off the solvent under low pressure. It can also be obtained by reacting anhydrous oxalic acid with ketene (H
2C=C=O).

Properties

Acetic oxalic anhydride is an unstable colorless crystalline solid, soluble in diethyl ether, that decomposes at about −3 °C into acetic anhydride (H
3C-(C=O)-)2O, carbon dioxide (CO
2) and carbon monoxide (CO). It is hydrolyzed by water into acetic and oxalic acids.

Acetic oxalic anhydride was conjectured to be an intermediate in the decomposition of anhydrous oxalic acid by acetic anhydride.

See also

References

  1. ^ W. R. Edwards and Walter M. Henley (1953), Acetic Oxalic Anhydride. J. Am. Chem. Soc., volume 75, issue 14, pages 3857-3859. doi:10.1021/ja01110a505
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