Ethylenetetracarboxylic dianhydride

Ethylenetetracarboxylic dianhydride
Names
	Preferred IUPAC name 1H,3H-Furo[3,4-c]furan-1,3,4,6-tetrone
Identifiers
CAS Number	15016-12-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	57437194;
PubChem CID	12651153;
UNII	MHG9QKW2DD ;
CompTox Dashboard (EPA)	DTXSID80505725 ;
	InChI InChI=1S/C6O6/c7-3-1-2(5(9)11-3)6(10)12-4(1)8 Key: GBASTSRAHRGUAB-UHFFFAOYSA-N;
	SMILES O=C(C(C(O2)=O)=C1C2=O)OC1=O;
Properties
Chemical formula	C6O6
Molar mass	168.060 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Ethylenetetracarboxylic dianhydride is a chemical compound with formula C
₆O
₆, that can be seen as the twofold anhydride of ethylenetetracarboxylic acid C
₆H
₄O
₈. It has a bicyclic molecular structure consisting of two maleic anhydride rings fused by their respective alkene units. It is a pale yellow oily liquid, soluble in dichloromethane and chloroform.^[1]

The compound^{[clarification needed]} and its reactions were first reported in 1967.^[2]^[3] More recently developed reactions for its synthesis include pyrolysis of ethylenetetracarboxylic acid^[4]

and microwave pyrolysis of solid Meldrum's acid.^[1] In this latter route, two molecules of the Meldrum's acid are believed to undergo a reductive dimerization to give an alkene linkage with one "Meldrum's acid" ring on each end. The rings then open via hydrolysis of the esters to form ethylenetetracarboxylic acid, and then the carboxylic acid units recyclize with different partners (cis on each side of the alkene) as in the simple pyrolysis of the tetraacid.

An alternative dianhydride isomer, consisting of two malonic anhydride units joined by an alkene,^[5] has not been reported in the literature.

References

^ ^a ^b Avat (Arman) Taherpour (2010), Microwave-assisted solid phase conversion study of Meldrum’s acid to ethylenetetracarboxylic dianhydride (C₆O₆) Spectrochimica Acta Part A, volume 75, pages 493–497 doi:10.1016/j.saa.2009.10.049
^ Jürgen Sauer, Barbara Schröder, Richard Wiemer (1967), Eine Studie der Diels-Alder-Reaktion, VI. Kinetischer Nachweis des Moleküls C₆O₆ (Dianhydrid der Äthylentetracarbonsäure). Chemische Berichte Volume 100 Issue 1, Pages 306-314 doi:10.1002/cber.19671000135
^ Jürgen Sauer, Barbara Schröder, Albrecht Mielert (1967), Eine Studie der Diels-Alder-Reaktion, VII. Reaktionen des Dianhydrids der Äthylentetracarbonsäure (C₆O₆). Chemische Berichte Volume 100 Issue 1, Pages 315-322 doi:10.1002/cber.19671000136
^ John M. Patterson, Nabeel F. Haidar, Loren L. Braun and Walter T. Smith, Jr. (1981), The pyrolytic behavior of ethylenetetracarboxylic acid. Journal of Analytical and Applied Pyrolysis, Volume 2, Issue 4, Pages 331-337 doi:10.1016/0165-2370(81)80005-8
^ CAS #160032-88-2

[taher-1] Avat (Arman) Taherpour (2010), Microwave-assisted solid phase conversion study of Meldrum’s acid to ethylenetetracarboxylic dianhydride (C₆O₆) Spectrochimica Acta Part A, volume 75, pages 493–497 doi:10.1016/j.saa.2009.10.049

[sauer1-2] Jürgen Sauer, Barbara Schröder, Richard Wiemer (1967), Eine Studie der Diels-Alder-Reaktion, VI. Kinetischer Nachweis des Moleküls C₆O₆ (Dianhydrid der Äthylentetracarbonsäure). Chemische Berichte Volume 100 Issue 1, Pages 306-314 doi:10.1002/cber.19671000135

[sauer2-3] Jürgen Sauer, Barbara Schröder, Albrecht Mielert (1967), Eine Studie der Diels-Alder-Reaktion, VII. Reaktionen des Dianhydrids der Äthylentetracarbonsäure (C₆O₆). Chemische Berichte Volume 100 Issue 1, Pages 315-322 doi:10.1002/cber.19671000136

[patt-4] John M. Patterson, Nabeel F. Haidar, Loren L. Braun and Walter T. Smith, Jr. (1981), The pyrolytic behavior of ethylenetetracarboxylic acid. Journal of Analytical and Applied Pyrolysis, Volume 2, Issue 4, Pages 331-337 doi:10.1016/0165-2370(81)80005-8

[5] CAS #160032-88-2

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[2]

[3]

[4]

[5]

Ethylenetetracarboxylic dianhydride

See also

References