The quest for odorants having salicylate notes

Flavour and Fragrance Journal - Tập 29 Số 2 - Trang 77-86 - 2014
Jean‐Marc Gaudin1
1Firmenich Aromatics Co., Ltd, Corporate R&D Division, No. 3901 Jindu Road, Xinzhuang Industry Park, Minhang District, Shanghai, China

Tóm tắt

ABSTRACTWe describe the synthesis and sensory characterization of a series of compounds which we anticipated would possess the olfactory notes of salicylates. We explored carba‐analogues, cyclic β‐keto esters and cyclic β‐diketones as salicylate analogues. Applying the simple concept of three‐dimensional structure similarity was very fruitful. Salicylate carba‐analogues and β‐keto esters, especially compounds 5, 7 and 10 for the first series and 27 and 28 for the second series, proved to be the most interesting type of compounds. For example, 1‐(2‐hydroxyphenyl)‐3‐phenyl‐1‐propanone (10), which can be found in nature, is nicely diffusive and has an excellent olfactory profile with an interesting dual floral–animal note. In general, these compounds may offer a first credible alternative to the popular salicylates. Copyright © 2013 John Wiley & Sons, Ltd.

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Tài liệu tham khảo

Bedoukian P., 1981, Perfum. Flavor., 6, 60

Clark G. S., 1999, Perfum. Flavor., 24, 5

10.1002/cbdv.200890090

Bauer K., 1990, Common Fragrance and Flavor Materials, 108

Kaiser R., 2006, Meaningful Scents Around the World, 165

Directive 2003/15/EC Off.J.Eur.Union L 66/26 11.3.2003.

10.1111/j.1600-0536.2010.01739.x

Couturier P. L., 1938, Action des de'rive's organomagne'siens mixtes, 559

10.1016/S0040-4039(01)00381-1

10.1002/hlca.19720550527

Ramanathan A., 2010, Synthesis, 217

Dow Chem. Co. U.S. Patent 2590813 1949.

Mallik U. K., 1990, J. Indian Chem. Soc., 67, 478

Tanaka H., 2002, Synlett, 9, 1427

10.1016/j.bmc.2003.12.026

10.1021/jo035395u

10.1021/jo062501u

10.1021/jo9709458

Blatt A. H., 1942, Organic Reactions, 344

10.1080/00304949209356226

10.1016/0040-4039(96)01706-6

10.1080/00397919908086090

10.1055/s-2004-829152

10.1002/chem.200900361

10.1055/s-2004-825603

10.1039/jr9600003575

Grasa G. A., 2004, Synthesis, 7, 971

Ogliaruso M. A., 1979, The Chemistry of Acid Derivatives, 267

10.1021/cr00020a004

Mascaretti O. A., 1997, Aldrichim. Acta, 30, 55

10.1002/(SICI)1099-0690(200004)2000:8<1633::AID-EJOC1633>3.0.CO;2-W

10.1002/ejoc.200500450

10.1055/s-2004-831309

10.1055/s-2000-6496

10.1021/jo01030a016

10.1016/0022-2860(90)85025-E

10.1139/v01-061

10.1016/S0040-4020(01)99345-7

10.1016/S0040-4020(01)83371-8

10.1021/jo00074a038

10.1021/ja00885a021

10.1002/cber.19570901217

10.1016/0040-4039(95)00481-Q

Pratap G., 1989, Fatigue materials: Advances and Emergences in Understanding, Proc. Symp. Mater. Sci. Technol., 91, 68