Lilac

1,3-Indandione (sometimes simply indanedione) is an organic compound with the molecular formula C₆H₄(CO)₂CH₂. It is a β-diketone with indane as its structural nucleus. It is a colorless or white solid, but old samples can appear yellowish^[3] or even green. It is a popular chemical scaffold (building block of various useful chemical compounds).^[4][5]

Structural properties

Solid 1,3-indandione is a diketone, As a solution in water, it is partially (~2%) enolized. The enolate anion exhibits significant delocalization, and the highest electron density is on the second carbon. This acid-base behavior explains many properties of the compound.^{[citation needed]}

Preparation

1,3-Indandione can be prepared by decarboxylation of the sodium salt of 2-ethoxycarbonyl-1,3-indandione, which itself is obtained by Claisen condensation of ethyl acetate and dimethyl phthalate.^{[citation needed]}

Chemical properties

The carbon at the C-2 position is alpha to both carbonyls, and thus can act as a nucleophile. It undergoes self-aldol condensation quite easily, resulting in bindone.

Bromination occurs at the 2-position:

One or both carbonyl groups can be reduced to alcohol groups or methylene groups, depending on the method used.

See also

• Vitamin K antagonist

References

External links

• Media related to 1,3-Indandione at Wikimedia Commons