- Source: 1,3-Indandione
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 or even green. It is a popular chemical scaffold (building block of various useful chemical compounds).
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.
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.
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