Pomarose

Pomarose
Names
	Preferred IUPAC name (2E,5Z)-5,6,7-Trimethylocta-2,5-dien-4-one
Identifiers
CAS Number	357650-26-1 ;
3D model (JSmol)	Interactive image;
ChemSpider	9205378 ;
PubChem CID	11030204;
UNII	EPU9H8QVS8 ;
CompTox Dashboard (EPA)	DTXSID00889170 ;
	InChI InChI=1S/C11H18O/c1-6-7-11(12)10(5)9(4)8(2)3/h6-8H,1-5H3/b7-6+,10-9- Key: QWRGOHMKGNCVAC-KQHSAVHASA-N ;
	SMILES O=C(/C(C)=C(C)\C(C)C)/C=C/C;
Properties
Chemical formula	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). verify (what is ?) 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 edit

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 edit

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.

Related compounds edit

Damascones

References edit

^ 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.
^ Swift, Karl, ed. (2002). Advances in flavours and fragrances: From the sensation to the synthesis. Cambridge: Royal Society of Chemistry. p. 138. ISBN 9780854048212.
^ 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.
^ Ohloff, Günther; Pickenhagen, Wilhelm; Kraft, Philip. (2012). Scent and Chemistry – The Molecular World of Odors. Zurich: Verlag Helvetica Chimica Acta. p. 217. ISBN 9783906390666.

[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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