Azulene

Azulene
Chemical name	bicyclo[5.3.0]decapentaene
Chemical formula	C10H8
Molecular mass	128.17 g/mol
Melting point	99 - 100 °C
Boiling point	242 °C
Density	g/cm3
CAS number	275-51-4
SMILES

Azulene is an organic compound whose molecules contain 10 carbons and 8 hydrogens and consist of a five-membered ring fused to a seven-membered ring. It is an isomer of naphthalene but its physical properties are quite different. Naphthalene is a white crystaline solid whereas azulene, whose name is derived from the Spanish word azul, meaning "blue", is a dark blue crystaline solid used in many cosmetics. Azulene has a long history dating back to the 15th century as the azure-blue distillate obtained by steam distillation of Chamomile. The compound was discovered and named in 1863 by Septimus Piesse in azure-blue distillates from other sources such as yarrow and wormwood. Lavoslav Ružička solved the structure for this compound and the first organic synthesis followed in 1937 by Placidus Plattner.

Derivatives

Vetivazulene or 4,8-dimethyl-2-isopropylazulene is obtained from vetiver oil. Guaiazulene or 1,4-dimethyl-7-isopropylazulene occurs naturally as a constituent of guaiac wood oil.

Structure

Azulene consists of a fused cyclopentadiene ring and a cycloheptatriene ring and is an isomer of naphthalene. Azulene is 10 pi electron system just like cyclodecapentaene and does have aromatic properties even though it is not a single ring system like benzene. The peripheral bonds have similar lengths and only the shared bond in the middle is a single bond. The stability gain from aromaticity is half of that of naphthalene. The molecule can be considered a fusion product of a 4 pi electron cyclopentadienide anion which is aromatic and the likewise aromatic 6 pi electron tropylium cation. The observed dipole moment of 1.0 Debye is consistent with this picture.

Organic synthesis

For many years not many synthetic routes existed to azulene and the compound was therefore expensive. A recent contribution takes cycloheptatriene as starting material ^[1].

Azulene procedure. step 1: cycloheptatriene 2+2 cycloaddition with dichloro ketene step 2: diazomethane insertion reaction step 3: dehydrohalogenation reaction with DMF step 4: carbonyl reduction to alcohol with sodium borohydride step 5: elimination reaction with Burgess reagent step 6: oxidation with p-chloranil step 7: dehalogenation with PMHS, palladium(II) acetate , potassium phosphate and the DPDB ligand

External links

• MSDS Website
• MSDS Website
• lab procedure for azulene from cyclopentadiene precursor Website

References

• ^  Approach to the Blues: A Highly Flexible Route to the Azulenes Sébastien Carret, Aurélien Blanc, Yoann Coquerel, Mikaël Berthod, Andrew E. Greene, Jean-Pierre Deprés Angewandte Chemie International Edition Volume 44, Issue 32 , Pages 5130 - 5133 2005 Abstract