Dienone - Wikipedia

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A dienone is a class of organic compounds with the general formula (R₂C=CR)₂C=O, where R is any substituent, but often H. They are formally "derived from 1,4-diene compounds by conversion of a –CH2– group into –C(=O)– group", resulting in "a conjugated structure". They are a kind of enone. The class includes some heterocyclic compounds.

The parent member is divinyl ketone. It is a colorless liquid (b.p. 38-40 °C) that tends to polymerize upon standing.^[1]

Dienones can arise via tautomerism of resorcinols and some hydroxypyridines.

Being multifunctional, dienones engage in many reactions. They are often good dienophiles. They function as ligands, forming metal-alkene complexes such as tris(dibenzylideneacetone)dipalladium(0).

Extensive work has been reported on cyclic dienones. The parent of the seven-membered ring series is tropone. It is a not only a dienone but a trieneone.

Cyclohexadienones are a significant class of dienones, the premier members being the ortho- and para-quinones. Many cyclohexadienones convert to phenols.^[2] In the dienone–phenol rearrangement, they convert to phenols^[3] through the dienone–phenol rearrangement:^[4]

The parent cyclopentadienone has only a fleeting existence under laboratory conditions, otherwise it dimerizes. The substituted derivative tetraphenylcyclopentadienone is however robust solid.^[5]

• Dione
• Penguinone