Squaramide

Squaramide is the organic compound with the formula O2C4(NH2)2. Not an amide in the usual sense, it is a derivative of squaric acid wherein the two OH groups are replaced by NH2 groups. Squaramides refer to a large class of derivatives wherein some of the H's are replaced by organic substituents. Exploiting their rigid planar structures, these compounds are of interest as hydrogen-bond donors in supramolecular chemistry and squaramide catalysis.[1] Squaramides exhibit 10-50x greater affinity for halides than do thioureas.[2] Squaramides also find application in medicinal chemistry, metabolomics and material science due to their ability to selectively conjugate amines[3][4]

Squaramide
Names
IUPAC name
3,4-diaminocyclobut-3-ene-1,2-dione
Identifiers
3D model (JSmol)
  • InChI=1S/C4H4N2O2/c5-1-2(6)4(8)3(1)7/h5-6H2
    Key: WUACDRFRFTWMHE-UHFFFAOYSA-N
  • C1(=C(C(=O)C1=O)N)N
Properties
C4H4N2O2
Molar mass112.088 g·mol−1
Appearancewhite solid
Melting point338–340 °C (640–644 °F; 611–613 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Squaramide is prepared by ammonolysis of diesters of squaric acid:[5][6]

O2C4(OEt)2 + 2 NH3 → O2C4(NH2)2 + 2 EtOH

N-Substituted squaramides are prepared similarly, using amines in place of ammonia.

Chloride-squaramide interaction in O2C4(NH(C6H4CF3)2. The characteristic planarity of a squaramide is evident.[2]

References