Contents

Tropone

Tropone^[1]

Names
Preferred IUPAC name Cyclohepta-2,4,6-trien-1-one
Other names Cyclohepta-2,4,6-trienone
Identifiers
CAS Number	539-80-0 Y
3D model (JSmol)	Interactive image
ChemSpider	10419 Y
ECHA InfoCard	100.007.933
PubChem CID	10881
UNII	CO48X7SUFH Y
CompTox Dashboard (EPA)	DTXSID60202169
InChI InChI=1S/C7H6O/c8-7-5-3-1-2-4-6-7/h1-6H Y Key: QVWDCTQRORVHHT-UHFFFAOYSA-N Y InChI=1/C7H6O/c8-7-5-3-1-2-4-6-7/h1-6H Key: QVWDCTQRORVHHT-UHFFFAOYAM
SMILES O=C\1/C=C\C=C/C=C/1
Properties
Chemical formula	C7H6O
Molar mass	106.12 g/mol
Density	1.094 g/mL
Boiling point	113 °C (235 °F; 386 K) (15 mmHg)
Hazards
Flash point	> 113 °C (235 °F; 386 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Chemical compound

Troponeor2,4,6-cycloheptatrien-1-one is an organic compound with some importance in organic chemistry as a non-benzenoid aromatic.^[2] The compound consists of a ring of seven carbon atoms with three conjugated alkene groups and a ketone group. The related compound tropolone (2-hydroxy-2,4,6-cycloheptatrien-1-one) has an additional alcohol (or an enol including the double bond) group next to the ketone. Tropones are uncommon in natural products, with the notable exception of the 2-hydroxyl derivatives, which are called tropolones.

Tropone has been known since 1951 and is also called cycloheptatrienylium oxide. The name tropolone was coined by M. J. S. Dewar in 1945 in connection to perceived aromatic properties.^[3]

Properties[edit]

Dewar in 1945 proposed that tropones could have aromatic properties. The carbonyl group is more polarized as a result of the triene ring, giving a partial positive charge on the carbon atom (A) and a partial negative charge on oxygen. In an extreme case, the carbon atom has a full positive charge (B) forming a tropylium ion ring which is an aromatic 6 electron system (C).

Tropones are also basic (D) as a result of the aromatic stabilization. This property can be observed in the ease of salt formation with acids. The dipole moment for tropone is 4.17 D compared to a value of only 3.04 D for cycloheptanone. This difference is consistent with stabilization of the dipolar resonance structure.

Synthesis[edit]

Numerous methods exist for the organic synthesis of tropones and its derivatives. Two selected methods for the synthesis of tropone are by selenium dioxide oxidationofcycloheptatriene^[4] and indirectly from tropinone by a Hofmann elimination and a bromination.^[2]

Reactions[edit]

Tropone undergoes ring contractiontobenzoic acid with potassium hydroxide at elevated temperature. Many derivatives also contract to the corresponding arenes.^[2] Tropone reacts in electrophilic substitution, for instance with bromine, but the reaction proceeds through the 1,2-addition product and is not an electrophilic aromatic substitution.^[2]

Tropone derivatives also react in nucleophilic substitution very much like in nucleophilic aromatic substitution.^[2]

Tropone is also found to react in an [8+3]annulation with a cinnamic aldehyde^[5]

Diene character[edit]

Tropone behaves as a diene in a Diels-Alder reactions, for instance with maleic anhydride.^[2] Similarly, it forms adducts with iron tricarbonyl, akin to (butadiene)iron tricarbonyl.^[6]

Derivatives[edit]

Name	Chemical structure	Natural sources
Tropolone		Pseudomonas lindbergii, Pseudomonas plantarii[7]
Hinokitiol		Cupressaceae trees[8]
Stipitatic acid		Talaromyces stipitatus[9]
Tropodithietic acid		Phaeobacter piscinae, Phaeobacter inhibens, Phaeobacter gallaeciensis[10][11]
Colchicine		Colchicum autumnale, Gloriosa superba[12]

Other tropone derivatives include puberulonic and puberulic acids, roseobacticides, pernambucone, crototropone, orobanone.^{[13][14][15][16][17]}

References[edit]