Pomarose
(2E,5Z)-Pomarose
Names
Preferred IUPAC name
(2E,5Z)-5,6,7-Trimethylocta-2,5-dien-4-one
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/C11H18O/c1-6-7-11(12)10(5)9(4)8(2)3/h6-8H,1-5H3/b7-6+,10-9- checkY
    Key: QWRGOHMKGNCVAC-KQHSAVHASA-N checkY
  • O=C(/C(C)=C(C)\C(C)C)/C=C/C
Properties
C11H18O
Molar mass 166.264 g·mol−1
Density 0.855 g/cm3
Boiling point 236.2 °C (457.2 °F; 509.3 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Pomarose is a high-impact captive odorant patented by Givaudan.[1] It is a double-unsaturated ketone that does not occur in nature. Pomarose has a powerful fruity rose odor with nuances of apples, plums and raisins, which is almost entirely due to the (2E,5Z)-stereoisomer, while its (2E,5E)-isomer is barely detectable for most people.[2] Catalyzed by traces of acids, both isomers equilibrate however quickly upon standing in glass containers.

Discovery and synthesis

5,6,7-Trimethylocta-2,5-dien-4-one was suspected by Philip Kraft et al.[3] by investigation of the NMR spectra of an unknown trace component with damascone odor in a crude complex reaction product. Although this trace component eventually turned out to be the constitutional isomer 2-methyl-3-isopropylhepta-2,5-dien-4-one. Pomarose was synthesized for structural curiosity and found to possess even superior fruity, rosy odor characteristics, reminiscent of apples, plums, raisins and other dried fruits with a low odor threshold of 0.5 ng/L air. The synthesis comprised borontrifluoride-catalyzed addition of methyl isopropyl ketone to 1-ethoxyprop-1-yne, which afforded ethyl 2,3,4-trimethylpent-2-enoate, and then was transformed into the target molecule by Grignard reaction with propen-1-ylmagnesium bromide via in situ enolization.

Use in perfumery

Pomarose has been used in a variety of perfumes.[4] It had its debut in Be Delicious for Men and it is also used in Unforgivable, 1 Million, CK free, Legend, Unforgivable Woman and John Galliano.

References

  1. ↑ Kraft, Philip (2001). "Preparation of 2-,5-,6-,7-,8-substituted oct-2-en-4-ones with odor and taste properties". Eur. Pat. Appl. 2001: EP 1149820 A1 20011031.
  2. ↑ Swift, Karl, ed. (2002). Advances in flavours and fragrances: From the sensation to the synthesis. Cambridge: Royal Society of Chemistry. p. 138. ISBN 9780854048212.
  3. ↑ Kraft, Philip; Denis, Caroline; Eichenberger, Walter (2001). "5,6,7-Trimethylocta-2,5-dien-4-one − A Suspected Odorant with Surprising Olfactory Properties". European Journal of Organic Chemistry. 2001 (12): 2363–2369. doi:10.1002/1099-0690(200106)2001:12<2363::AID-EJOC2363>3.0.CO;2-E.
  4. ↑ Ohloff, Günther; Pickenhagen, Wilhelm; Kraft, Philip. (2012). Scent and Chemistry – The Molecular World of Odors. Zurich: Verlag Helvetica Chimica Acta. p. 217. ISBN 9783906390666.
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