Title: Novel Fragrance Compounds

Field of the Invention

The invention relates to the discovery of novel fragrance compounds, and perfumes and perfumed products comprising the novel compounds.

Background

A major area of interest in the fragrance industry is to find high odour impact fragrance materials which can provide superior performance at lower concentrations giving cost- savings and lower environmental impact.

Muguet (Lily of the Valley) is an important area in perfumery (M Boelens and H Wobben, Perfumer & Flavorist, 1980, 5 (6), 1-8) and the odour is created by a combination of fragrance ingredients, of which 3 -(3 / 4-alkylphenyl)propanals such as Bourgeonal™ (3-(4-tert-butylphenyl)ρropanal, US 2,976,321), Florhydral™ (3-(3-isopropylphenyl)butanal, EP 368156), Lily aldehyde™ (3-4-tert-butylphenyl)-2-methylpropanal, US 2,875,131) and Cyclamen aldehyde™ (3-(4-isopropylphenyl)-2-methylpropanal, US 1,844,013) provide floral, green and in particular watery aspects. All of these materials are used in Muguet accords in high volumes to good effect.

The relationship between molecular structure and odour has intrigued and perplexed scientists for two and a half millennia since Democritus and Epicurus first postulated a causal relationship among philosophical circles in Athens. The ability to accurately and consistently predict the odour of putative molecules from their molecular structure continues to prove elusive. Recent developments (which led to the award of a Nobel Prize) in molecular biology have now given an insight into the reasons behind this. Discovery of the gene family encoding for olfactory receptor proteins (L. B. Buck and R. Axel, Cell, 1991, 65, 175-187) paved the way for confirmation that the sense of smell is combinatorial in nature and uses an array of hundreds of different receptor types. (B. Malnic, J. Hirono, T.-

Sato and L. B. Buck, Cell, 1999, 96, 713-723) Some of the issues raised by this in terms of odorant design axe described by no less a figure than another Nobel Laureate E. J. Corey in a paper on the understanding of odorant-receptor interaction. (S. Hong and E. J. Corey, J. Amer. Chern. Soc, 2006, 128, 1346-1352). A review on the subject shows that, far from making rational odorant design easier, this new understanding indicates that accurate and consistent prediction of odour properties will remain beyond our grasp for the foreseeable future. (C. S. Sell, Angew. Chem. Int. Edn., 2006, 45, 6254-6261) Furthermore, an essay on property prediction from molecular structure (M. Jansen and J. C. Schoen, Angew. Chem. Int. Edn., 2006, 45, 3406-3412) suggests that, at an even deeper level, all chemical properties of a proposed structure are not accurately and consistently predictable.

In a study made by R Pelzer et al (R Pelzer, U Harder, A Krempel, H Sommer, S Surburg and P Hoever in Recent Developments in Flavour & Fragrance Chemistry - Proceedings of the 3 ^rd International Haarmann & Reimer Symposium, Ed R Hopp and K Mori, VCH, 1993 pp 29 - 67), 181 substances possessing different aspects of the Lily of the Valley fragrance were investigated with the use of computer models. For the aldehydic materials, 41 in total, the generic fragment structure

was developed and it was stated, amongst other requirements, that "a double bond at C-4 is ^' particularly advantageous, and may also be part of an aromatic system".

There are a smaller number of aldehydic materials that are non-aromatic and possess Muguet-like odours but these tend to have alicyclic terpinoid-like structures such as Trimenal.

EP 1054053 A discloses non-aromatic aldehydes with the generic structure of:

where R = H or Me, the dotted line representing either a double or single bond and n = 0 (when dotted line represents a single bond) and 1 (when the dotted line represents a double bond). In the latter case, the material was described as having an aldehydic, flowery-lily of the valley, fatty type of odour with a Lily aldehyde™/Bourgeonal™ connotation but is described as definitely more floral, more white flower than that of Lily aldehyde™. This molecule also fits the Pelzer model in that unsaturation is present at the C-4 position.

3-(3-methylcyclohexyl)propanal is disclosed in "Sur I 'addition radiculaire d'acide bromhydrique, sur quelques composes allyliques cycloniques en presence de peroxyde de diterbutyle. Reactions de substitution sur les bromures", J-M Pabiot and R Pallaud, C. R. Acad. Sc. (1971), 273(6), 475-7. However no odour properties are disclosed.

Summary of the invention

Surprisingly we have found that 3-(3-alkylcyclohexyl)propanals provide a higher odour impact relative to the commercially available substituted 3-(3/4-alkylphenyl)propanals. This result is unexpected, since it is commonly known that Muguet (Lily of the Valley) odorants based on aldehydic functionality have defined structural requirements, in particular, unsaturation in the six-membered ring.

Thus, in a first aspect, the invention provides a compound having the structure

(Formula 1)

where R ₁ is C ₁ to C ₅ alkyl and R ₂ to R ₅ are independently selected from H and methyl, with the proviso that when R ₂ to R ₅ are each H then Ri is not methyl.

In a second aspect, the invention provides a perfume comprising the compound of Formula 1 where Ri is Ci to C ₅ alkyl, and R ₂ to R ₅ are independently selected from H and methyl.

In a third aspect, the invention provides use of a compound of Formula 1 where Ri is Ci to C ₅ alkyl, and R ₂ to R ₅ are independently selected from H and methyl, for use as a perfumery ingredient.

Such novel aldehyde compounds have been surprisingly found to have a strong and pleasant ^" odour and are suitable for use as perfume ingredients, particularly in Muguet accords/ fragrances.

Preferably Ri is selected from isopropyl, tert-bntyl, see-butyl, iyo-butyl, 2,2-dimethylpropyl.

Preferred materials are where at least one of R ₂ and R ₃ is H and at least one Of R ₄ and R ₅ is H. A particularly preferred compound is where Ri is tert-buty\ and R ₂ to R ₅ are each H.

The odour properties of the aldehydes of the invention mean that an aldehyde, (including corresponding acetals or Schiffs bases), or mixture of aldehydes in accordance with the invention, may be used as such to impart, strengthen or improve the odour of a wide variety of products, or may be used as a component of a perfume (or fragrance composition) to contribute its odour character to the overall odour of such perfume.

For the purposes of this invention a perfume means a mixture of fragrance materials, if desired mixed with or dissolved in a suitable solvent or mixed with a solid substrate.

The quantities in which one or more aldehydes according to the invention can be used in perfumes may vary within wide limits and depend, inter alia, on the nature and the quantity of the other components of the perfume in which the aldehyde is used and on the olfactive effect desired. It is therefore only possible to specify wide limits, which, however, provide-

sufficient information for the specialist in the art to be able to use an aldehyde according to the invention for his specific purpose. Typically, a perfume comprises one or more aldehydes in accordance with the invention in an olfactively effective amount. In perfumes an amount of 0.01% by weight or more of an aldehyde according to the invention will generally have a clearly perceptible olfactive effect. Preferably the amount is from 0.1 to 80% by weight, more preferably at least 1% by weight.

In a further aspect, the invention provides a perfumed product comprising a novel compound or perfume disclosed herein.

Example of such products are: fabric washing powders, washing liquids, fabric softeners and other fabric care products; detergents and household cleaning, scouring and disinfection products; air fresheners, room sprays and pomanders; soaps, bath and shower gels, shampoos, hair conditioners and other personal cleansing products; cosmetics such as creams, ointments, toilet waters, pre-shave, aftershave, skin and other lotions, talcum powers, body deodorants and antiperspirants, etc.

The amount of the aldehyde according to the invention present in products will generally be at least 10 ppm by weight, preferably at least 100 ppm, more preferably at least 1000 ppm. However, levels of up to about 20% by weight may be used in particular cases, depending on the product to be perfumed.

It has also been surprisingly discovered that certain aldehydes in accordance with the invention show good substantivity to hair and cloth, both wet and dry, and hence have good potential for use in fabric treatment products and hair care products.

It has also been surprisingly discovered that aldehydes in accordance with the invention have antibacterial and antimicrobial properties, rendering them particularly suitable for inclusion in products as described above. In particular 3-(3-tert-butylcyclohexyl)propanal has been found to have excellent activity against Staphylococcus aureus. In addition, isomers of this material (e.g. 3-(3-isopropylcyclohexyl)butanal) have also been found to have excellent activity against Staphylococcus aureus, and may have some use in antibacterial fragrance technology in some applications.

A further surprising property of certain aldehydes of the present invention is the ability to possess insect repellency properties. In particular it has been found that 3-(3-tert- butylcyclohexyl)propanal has excellent repellency properties against mosquitoes and ants.

A further surprising property of certain aldehydes of the present invention is the ability to act as a malodour counteractant. In particular, 2-methyl-3-(3-methylcyclohexyl)propanal, 3-(3- methylcyclohexyl)propanal and 3-(3-tert-butylcyclohexyl)propanal were found to be particularly good malodour counteractants, especially against bathroom malodour.

Preparation

The compounds according to the invention may be prepared according to procedures known in the art. The 3-(3-alkylcyclohexyl)propanals may be prepared in two stages from the corresponding 3-(3-alkylphenyl)propanals. Firstly, the phenyl ring may be hydrogenated using catalytic techniques typically used for hydrogenation of substituted benzene (RL Augustine in Heterogeneous Catalysis for the Synthetic Chemist, 1996, Marcel Dekker Inc., New York, ISBN 0-8247-9021-9, pp 403-437). This hydrogenation technique will typically also hydrogenate the aldehyde function of 3-(3-alkylphenyl)propanals and thus the product produced will be 3-(3-alkylcyclohexyl)propan-l-ols. Therefore secondly, the resultant alcohols are typically oxidised back to the aldehyde using stoichiometric oxidants such as l,l,l-Tris(acetyloxy)-l,l-dihydro-l,2-benziodoxol-2-(lH)-one (Dess-Martin periodinane) or catalytic vapour phase dehydrogenation using catalysts such as copper chromite at 200-. 25O ⁰ C, under 30mBar.

Alternatively the 3-(3-alkylcyclohexyl)propanals may be prepared in three stages from the corresponding 3-(3-alkylphenyl)propanals via acetalisation. Firstly, the aldehyde function is converted to an acetal by reaction with an alcohol or suitable diol according to procedures known in the art. A generic example of a resultant acetal from ethylene glycol is

Secondly, the phenyl ring may be hydrogenated using catalytic techniques typically used for hydrogenation of substituted benzene to yield the acetal of 3-(3-alkylcyclohexy)propanal Thirdly, the acetal is hydrolysed using procedures known in the art (S Sen et al J. Org. Chem. 1997, 62, 6684-86) to obtain the target 3-(3-alkylcyclohexyl)propanal.

The 3-(3-alkylcyclohexyl)propanals according to the invention are generally obtained as mixtures of cis and trans isomers (R ₁ and the propanal side chain are on the same side or opposite side of the cyclohexyl ring respectively). This cis/trans ratio is dependent upon the synthesis procedure used and more particularly, dependent upon the hydrogenation procedure. Generally, the odours of both isomers are different and the isomers may be separated by procedures known in the art such as column chromatography, fractional distillation and gas chromatography. The isomers may be used separately as fragrance materials or the isomer mixture obtained from the synthetic procedure may be used as such, depending on which particular odour character or mixture of odour characters is preferred for a particular application.

Also, the 3-(3-alkylcyclohexyi)propanals according to the invention exist in various stereoisomeric forms. They are obtained by the synthetic procedures described above as racemic mixtures, which may be separated into the various stereoisomers by procedures known in the art, particularly by gas chromatography using chiral columns. Therefore, the invention provides the 3-(3-alkylcyclohexyl)propanals as cis/trans and stereoisomeric mixtures as well as the various cis and trans and stereoisomers separately and includes the- use of these separate isomers as fragrance materials.

Other fragrance materials

Other fragrance materials which can be advantageously combined with one or more aldehydes according to the invention in a perfume are, for example, natural products such as extracts, essential oils, absolutes, resinoids, resins, concretes etc., but also synthetic materials such as hydrocarbons, alcohols, aldehydes, ketones, ethers, acids, esters, acetals, ketals, nitriles, etc., including saturated and unsaturated compounds, aliphatic, carbocyclic, and heterocyclic compounds.

Such fragrance materials are mentioned, for example, in S. Arctander, Perfume and Flavor Chemicals (Montclair, NJ., 1969), in S. Arctander, Perfume and Flavor Materials of Natural Origin (Elizabeth, NJ., 1960), "Flavor and Fragrance Materials - 1991"\ Allured Publishing Co. Wheaton, IU. USA and in H Surburg and J Panten, "Common Fragrance and Flavor Materials", Wiley-VCH, Weinheim, 2006 ISBN-13: 978-3-527-31315-0, ISBN-IO: 3-527- 31315-X.

Examples of fragrance materials which can be used in combination with one or more aldehydes according to the invention are: geram ^' ol, geranyl acetate, linalool, linalyl acetate, tetrahydrolinalool, citronellol, citronellyl acetate, dihydromyrcenol, dihydromyrcenyl acetate, tetrahydromyrcenol, terpineol, terpinyl acetate, nopol, nopyl acetate, 2-phenyl- ethanol, 2phenylethyl acetate, benzyl alcohol, benzyl acetate, benzyl salicylate, styrallyl acetate, benzyl benzoate, amyl salicylate, dimethylbenzyl-carbinyl acetate, trichloro- methylphenyl-carbήiyl acetate, p-tert-butylcyclohexyl acetate, isononyl acetate, vetiveryl acetate, vetiverol, αhexylcinnamaldehyde, 2-methyl- 3-(p-tert -butylphenyl) prop anal, 2-methyl-3-(p-isopropylphenyl)ρroρanal, 2-(p-tert-butylρhenyl)-propanal, 2,4-dimethyl- cyclohex-3-enylcarboxaldehyde, tricyclodecenyl acetate, tricyclodecenyl propionate, ^' 4-(4-hydroxy-4methylpentyl)-3-cyclohexenecarboxyaldehyde, 4-(4-methyl-3-pentenyi)- 3-cyclohexenecarboxaldehyde, 4-acetoxy-3-ρentyltetrahydropyran, 3-carboxy methyl- 2-ρentylcyclopentanone, 2-n-heptylcyclopentanone, 3-methyl-2-pentyl-2-cyclopentenone, n-decanal, n-dodecanal, 9-decenol-l, phenoxyethyl isobutyrate, phenylacetaldehyde dimethylacetal, phenylacetaldehyde diethyl acetal, geranyl nitrile, citronellyl nitrile, cedryl- acetate, 3isocamphylcyclohexanol, cedryl methyl ether, isolongifolanone, aubepine nitrile, anisic aldehyde, heliotropin, cournarin, eugenol, vanillin, diphenyl oxide, hydroxycitronellal, ionones, methylionones, isomethylionones, irones, cis-3-hexenol and esters thereof, indane musks, tetralin musks, isochroman musks, macrocyclic ketones, macrocyclic lactone musks, ethylene brassylate.

Solvents which can be used for perfumes which contain an aldehyde according to the invention are, for example: ethanol, isopropanol, diethyleneglycol mono ethyl ether, dipropylene glycol, diethyl phthalate, triethyl citrate, isopropyl myristate, etc.

The invention will be further described, by way of illustration in the following examples.

Example 1 - Preparation of 3-(3-methylcvclohexyl)propanal

i) 3-(3-methylcyclohexyi)propan-l-ol

5% Ru/ Al ₂ O ₃ (3g, 5wt%), (2£)-3-(3-methylphenyl)acrylic acid (6Og, 0.37mol) and acetic acid (30OmL) were charged into a 50OmL autoclave vessel. The mixture was vigorously stirred under a hydrogen atmosphere (40bar) at 15O ⁰ C, for 3 days. The catalyst was filtered and the product was dissolved in ethyl acetate (50OmL), washed with water (50OmL) and brine (50OmL). The organic phase was dried over sodium sulphate, filtered and evaporated to yield crude 3-(3-methylcyclohexyl)propanoic acid (6Og, 0.35mol, 95% yield) as a colourless oil.

LiAlH ₄ (16g, 0.42mol, 1.2eq) and diethyl ether (45OmL) were charged into a 2L three- necked round-bottom flask equipped with a mechanical stirrer and a reflux condenser and cooled at O ⁰ C. The crude 3-(3-methylcyclohexyl)propanoic acid (6Og, 0.35mol) was dissolved in diethyl ether (40OmL) and added dropwise to the reaction flask. The reaction mixture was then stirred for 3h at ambient temperature. The excess of lithium aluminium hydride was hydrolyzed with saturated aqueous sodium sulphate and the mixture filtered. THF (IL) was added to the residue and the suspension was heated to 35 ⁰ C for Ih. The suspension was filtered and the combined organic layers were dried over sodium sulphate and evaporated to yield the crude product as an oil. Chromatography on a silica gel column with 8% EtOAc in hexane as elution agent, followed by a bulb-to-bulb distillation (O. lmBar, 14O ⁰ C) gave pure 3-(3-methylcyclohexyl)propan-l-ol (35g, gc purity > 98 % ; yield = 61 %).

Odour: aldehydic, watery, fatty, citrus, nitrile.

Analytical data (predominantly one isomer):

¹ H NMR (400 MHz, CHLOROFORM-rf) ppm: 0.46-1.72 (m, 15H); 0.85 (d, 3H); 3.57- 3,64 (m, 2H).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 22.93 (q, 1C); 26.29 (t, 1C); 30.12 (t, 1C); 32.67 (d, 1C); 32.92 (t, 1C); 33.49 (t, 1C); 35.31 (t, 1C); 37.49 (d, 1C); 42.28 (t, 1C); 63.38 (t, 1C).

MS: m/z (relative intensity): 156 (M ⁺ , < 1), 138 (5), 123 (5), 110 (44), 97 (46), 96 (27), 95 (100), 82 (52), 81 (42), 69 (15), 67 (23), 55 (84), 41 (23).

ii) 3-(3-methylcyclohexyl)propanal

In a 2L three-necked round-bottom flask equipped with a mechanical stirrer and a reflux condenser were introduced a solution of 3-(3-methylcyclohexyl)propan-l-ol (23.3g, 0.15mol) in dichloromethane (14OmL), a solution of potassium bromide (1.77g, 15mmol, O.leq) in water (25mL) and 2,2,6,6-tetramethyl-l-piperidrnyloxy (TEMPO, 300mg, 1.92mmol, O.Oleq). To this mixture was added 0.35M aqueous sodium hypochlorite (594mL). The mixture was stirred for 3 days at 35 ⁰ C then extracted with dichloromethane (50OmL). The organic layer was washed with water (30OmL), IN HCl (30OmL) and brine (30OmL), dried over sodium sulphate and concentrated. The crude product was chromatographed on silica gel with 8% EtOAc in hexane as elution agent, followed by a bulb-to-bulb distillation (O.OlmBar, 79 ⁰ C) to give pure 3-(3-methylcyclohexyl)propanal (11.8g, gc purity > 98%; yield = 51 %).

Odour: aldehydic, fatty, nitrile.

Analytical data (predominantly one isomer):

¹ H NMR (400 MHz, CHLOROFORM-^) ppm: 0.45-1.75 (m, 12H); 0.84 (d, 3H); 2.38- 2.44 (m, 2H); 9.73 (t, IH).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 22.81 (q, 1C); 26.08 (t, 1C); 29.40 (t, 1C); 32.53 (d, 1C); 32.57 (t, 1C); 35.08 (t, 1C); 37.16 (d, 1C); 41.48 (t, 1C); 41.86 (t, 1C); 203.03 (d, 1C).

MS: m/z (relative intensity): 154 (M ⁺ , < 1), 136 (12), 121 (15), 110 (28), 108 (39), 97 (27), 95 (100), 82 (72), 81 (39), 69 (19), 68 (20), 67 (27), 55 (86), 41 (33).

Example 2 - Preparation of 3-(3-fgr?-butylcyclohexyDpropanal

i) l-(l-bromoethyl)-3-te/?-butylbenzene

A solution of l-tert-butyl-3-ethylbenzene (90g, 0.54mol) in carbon tetrachloride (600 mL) was charged into a 2L three-necked round-bottom flask, equipped with a mechanical stirrer and a reflux condenser. The reaction was stirred vigorously while N-bromosuccinimide (97.6g, 0.54mol, leq) was added, followed by benzoyl peroxide (0.8g, 2.23mmol,- 0.004eq). The reaction mixture was then heated to mild reflux for Ih. Once cooled, the mixture was filtered and the organic phase was washed successively with water (2x300mL), 10% Na ₂ SO ₃ water solution (15OmL), water (2x300mL) and a saturated NaHCO ₃ water solution (10OmL), dried over magnesium sulphate and concentrated.

Unreacted l-teτt-butyl-3-ethylbenzene was removed by fractional distillation (8.2mBar, 79- 80 °C) to leave l-(l-bromoethyl)-3-rerϊ-butylbenzene (132g, gc purity > 90%; yield = 95%), which was used as such for the next step.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 1.38 (s, 9H); 2.10 (d, 3H); 5.27 (q, IH); 7.32-7.48 (m, 4H).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 26.97 (q, 1C); 31.29 (q, 3C); 34.70 (s, 1C); 50.25 (d, 1C); 123.79 (d, 1C); 123.81 (d, 1C); 125.41 (d, 1C); 128.35 (d, 1C); 142.81 (s, 1C); 151.47 (s, 1C).

MS: m/z (relative intensity): (no M ⁺ ), 227 (2), 225 (2), 161 (100), 145 (14), 131 (10), 117 (19), 105 (12), 91 (18), 77 (10), 57 (65), 41 (20), 39 (14).

ii) l-?ert-butyl-3-vinylbenzene

Potassium hydroxide (140.9g, 2.51mol, 1.9eq), l-(l-bromoethyl)-3-terr-butylbenzene (347.12g, 90.9% gc pure, 1.31mol, leq) and 2-propanol (2.6kg) were charged into a 5L three-necked round-bottom flask, equipped with a mechanical stirrer and a reflux condenser. After stirring for 2h at 60 ⁰ C, the reaction mixture was cooled to ambient temperature and poured into ice (1.7kg), and the product was extracted with pentane (1.5L). The organic phase thus obtained was washed twice with water (75OmL portions) and a saturated NaHCO ₃ water solution (30OmL), dried over Magnesium sulphate and concentrated. The crude product was chromatographed on a silica gel column with hexane as elution agent to give the product as a colourless oil (119.6g, gc purity of 93 %), which was stabilised with 0.3g of BHT. Flash distillation using a Vigreux column (3.4mBar, 60- 64°C) gave l-te^butyl-3-vinylbenzene (105.3g, gc purity> 97% , yield = 50%).

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 1.37 (q, 9H); 5.27 (d, IH); 5.78 (d, IH); 6.77 (dd, IH); 7.28 - 7.35 (m, 3H); 7.45 (s, IH).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 31.31 (q, 3C); 34.62 (s, 1C); 113.42 (t, 1C); 123.17 (d, 1C); 123.42 (d, 1C); 124.92 (d, 1C); 128.23 (d, 1C); 137.22 (s, 1C); 137.35 (d, 1C); 151.30 (s, 1C).

MS: m/z (relative intensity): 160 (M ⁺ , 19), 145 (100), 128 (12), 117 (56), 115 (19), 105 (17), 91 (16), 77 (10), 63 (6), 57 (7), 51 (8), 41 (8), 39 (13).

iii) 3-(3-tert-butylphenyl)propanal

Acetylacetonatodicarbonylrhodium (I) (41mg, 0.1mol%) of l-te^butyl-3-vinylbenzene (29g, 0.16mol) and a solution of triphenylphosphite (261mg, 0.99mmol) in 88g of toluene were added to a 25OmL autoclave vessel. The vigorously stirred reaction mixture heated for 6h under a pressure of syn gas (mixture of hydrogen and carbon monoxide in a ratio ^' 1: 1 - IBar), at 80 ⁰ C. The crude reaction mixture was concentrated in vacuo and chromatographed on a silica gel column with 3 % MTBE in hexane as elution agent to give 3-(3-ϊerϊ-butylphenyl)propanal (24.5g, gc purity > 82%; yield = 63%).

Odour: aldehydic, floral, rubber.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 1.35 (s, 9H); 2.81 (t, 2H); 2.96 (t, 2H); 7.01-7.30 (m, 4H); 9.85 (d, IH).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 28.32 (t, 1C); 31.29 (q, 3C); 34.54 (s, 1C); 45.35 (t, 1C); 123.21 (d, 1C); 125.22 (d, 1C); 125.27 (d, 1C); 128.22 (d, 1C); 139.87 (s, 1C); 151.41 (s, 1C); 201.57 (d, 1C).

MS: m/z (relative intensity): 190 (M ⁺ , 32), 175 (82), 172 (0.5), 157 (4), 147 (12), 133 (21), 131 (100), 119 (11), 117 (12), 116 (11), 115 (17), 105 (16), 91 (26), 77 (10), 65 (5), 57 (17), 41 (9).

iv) 2-[2-(3-te^butylphenyl)ethyl]-l,3-dioxolane

Ethylene glycol (15mL, 0.27mol, 1.2eq), paratoluene sulfonic acid (430mg, 1 % w/w) and cyclohexane (5OmL) were charged into a IL three-necked round-bottom flask, equipped with a dean and stark, a reflux condenser and a mechanical stirrer. 3-(3-tert- butylphenyl)propanal (50.6g, gc purity of 85 %, 0.22mol) was added dropwise at ambient temperature. After stirring for 2h at reflux, the reaction mixture was cooled to ambient temperature and washed twice with water (5OmL), saturated aqueous NaHCO ₃ , dried over magnesium sulphate and concentrated to give 2-[2-(3-fe?t-butylphenyl)ethyl]-l,3-dioxolane in the form of a pale yellow coloured oil (6Og, gc purity > 84%; yield > 95%). The material was used as such for the next step.

Odour: floral, aldehydic, muguet, linalool.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-rf) ppm: 1.33 (s, 9H); 2.03 (m, 2H); 2.75 (m, 2H); 3.87-5.05 (m, 4H); 4.93 (t, IH); 7.05 (m, IH); 7.25 (m, 3H).

¹³ C NMR (101 MHz, CHLOROFORM-rf) ppm: 30.37 (t, 1C); 31.35 (q, 3C); 34.56 (s, 1C); 35.64 (t, 1C); 64.91 (t, 2C); 103.91 (d, 1C); 122.79 (d, 1C); 125.41 (d, 2C); 128.02 (d, 1C); 141.13 (s, 1C); 151.16 (s, 1C).

MS: m/z (relative intensity): 234 (M ⁺ , 7), 219 (1), 191 (3), 172 (17), 157 (12), 148 (11), 147 (13), 133 (32), 131 (24), 117 (16), 115 (16), 105 (13), 100 (40), 92 (43), 91 (22), 87 (41), 77 (6), 73 (100), 57 (48), 45 (20).

v) 2-[2-(3-ferf-butylcycloliexyl)ethyl]-l ,3-dioxolane

5% Ru/ Al ₂ O ₃ (3g, 5% w/w) were charged into a 10OmL autoclave vessel with 2-[2-(3-tert- butylphenyl)ethyl]-l,3-dioxolane (6Og, gc purity of 84%, 0.21mol). The mixture was vigorously stirred under an hydrogen atmosphere (60Bar) at 130 ⁰ C for 4h. The reaction mixture was filtered, rinsed with cyclohexane and concentrated to give 2-[2-(3-tert- butylcyclohexyl)ethyl]-l,3-dioxolane in the form of a pale yellow coloured oil (62.1g, gc purity > 87%; yield > 99%). The material was used as such for the next step.

Odour: floral, muguet, citrus, salicylate, minty.

Analytical data (predominantly one isomer):

¹ H NMR (400 MHz, CHLOROFORM-ύQ ppm: 0.50-1.80 (m, 14H); 0.79 (s, 9H); 3.76- 3.93 (m,4H); 4.79 (t, IH).

¹³ C NMR (101 MHz, CHLOROFORM-^) ppm: 26.63 (t, 1C); 27.30 (t, 1C); 27.49 (q, 3C); 31.35 (t, 1C); 31.87 (t, 1C); 32.41 (s, 1C); 33.08 (t, 1C); 34.27 (t, 1C); 38.03 (d, 1C); 47.91 (d, 1C); 64.76 (t, 2C); 104.91 (d, 1C).

MS: m/z (relative intensity) 240 (M ⁺ , < 1), 239 (1), 183 (1), 163 (3), 121 (7), 95 (4), 81 (4), 79 (4), 73 (100), 67 (5), 57 (10), 45 (7), 41 (8).

vi) 3-(3-?e/t-butylcycloliexyl)propaiial

2-[2-(3-ϊe^butylcyclohexyl)etiiyl]-l,3-dioxolane (62g, 0.22mol, gc purity of 87%) and dichloromethane/acetone in a 4: 1 ratio (3.7L) were charged into a 5L three-necked round- bottom flask equipped with a reflux condenser and a mechanical stirrer. Iron (III) chloride hexahydrate (212.3g, 0.78mol, 3.5eq) was added to the reaction at ambient temperature. The reaction mixture was then stirred at ambient temperature for 4h and subsequently quenched, at 5-10 ⁰ C, with the addition of a saturated aqueous NaHCO ₃ (50OmL). The organic phase was then washed with brine (50OmL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled via a Vigreux column (0.5mBar, 82-85 ⁰ C), to give colourless oil (34.7g, gc purity 79%). The oil was chromatographed on a silica gel column with 2% EtOAc in hexane as elution agent giving 3-(3-tert- butylcyclohexyl)propanal (17.8g, gc purity > 98%, ratio cis:trans 75:25; yield 40%).

Odour: aldehydic, floral, muguet, green.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-^) ppm: 0.52-0.86 (m, 3H), 0.80 (s, 9H), 0.82 (s, 9H), 0.84-1.79 (m, 21H), 2.34-2.42 (m, 2H), 2.43 (td, 2H, J=7.63, 1.83 Hz), 9.75 (t, IH, /= 1.95 Hz), 9.77 (t, IH, /= 1.83 Hz).

¹³ C NMR (101 MHz, CHLOROFORM-^) ppm: 21.36 (t, 1C), 23.70 (t, 1C), 26.51 (t, 1C), 27.19 (q, 3C), 27.32 (q, 3C), 27.50 (t, 1C), 27.57 (t, 1C), 29.62 (t, 1C), 29.72 (t, 1C), 30.84 (t, 1C), 32.25 (s, 1C), 32.44 (s, 1C), 32.83 (t, 1C), 33.16 (d, 1C), 34.18 (t, 1C), 37.69 (d, 1C), 41.37 (d, 1C), 41.58 (t, 1C), 42.61 (t, 1C), 47.84 (d, 1C), 203.00 (d, 1C), 203.10 (d, 1C).

Pure CIS-isomer:

Odour: aldehydic, floral, muguet, watery.

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 0.52-0.67 (m, H); 0.76-0.86 (m, 2H); 0.82 (s, 9H); 0.94-1.02 (m, IH); 1.12-1.25 (m, 2H); 1.47-1.57 (m, 2H); 1.65-1.79 (m,- 4H); 2.43 (td, 2H, /=7.63, 1.83 Hz); 9.75 (t, IH, /= 1.95 Hz).

¹³ C NMR (101 MHz, CHLOROFORM-rf) ppm: 26.51 (t, 1C); 27.19 (q, 3C); 27.50 (t, 1C); 29.72 (t, 1C); 32.44 (s, 1C); 32.83 (t, 1C); 34.18 (t, 1C); 37.69 (d, 1C); 41.58 (t, 1C); 47.84 (d, 1C); 203.10 (d, 1C).

MS: m/z (relative intensity) (no M ⁺ ), 163 (7), 152(3), 139 (29), 121 (28), 109 (3), 107 (5), 95 (26), 81 (25), 79 (20), 69 (12), 67 (23), 57 (100), 41 (41).

Pure TRANS-isomer:

Odour: aldehydic, floral, metallic.

¹ H NMR (400 MHz, CHLOROFORM-^ ppm: 0.80 (s, 9H); 0.84-0.96 (m, IH); 1.05- 1.21 m, (2H); 1.30-1.43 (m, 2H); 1.43-1.55 (m, 2H); 1.55-1.63 (m, IH); 1.64-1.79 (m, 4H); 2.34-2.42 (m, 2H); 9.77 (t, IH, J= 1.83 Hz).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 21.36 (t, 1C); 23.70 (t, 1C); 27.32 (q, 3C); 27.57 (t, 1C); 29.62 (t, 1C); 30.84 (t, 1C); 32.25 (s, 1C); 33.16 (d, 1C); 41.37 (d, 1C); 42.61 (t, 1C); 203.00 (d, 1C).

MS: m/z (relative intensity) (no M ⁺ ), 163 (4), 152 (6), 139 (34), 121 (28), 109 (5), 107 (5), 95 (30), 81 (27), 79 (22), 69 (12), 67 (24), 57 (100), 41 (45).

Example 3 -Preparation of 3-(3-methylcyclohexyl)butanal

i) 3-(3-methylphenyl)butanal

In a IL three-necked round-bottom flask equipped with a mechanical stirrer and a reflux condenser were introduced DMF (30OmL), 3-bromo toluene (66.3g, 0.39mol), of crotyl alcohol (99mL, 1.16mol, 3eq), sodium carbonate (102.5g, 0.97mol, 2.5eq), tetrabutyl- ammonium bromide (107.6g, 0.39mol, leq), palladium acetate (7.8g, ll.δmmol, 3mol%) and tri-o-tolyl phosphine (11.8g, 38.7mmol, O.leq). After stirring for Ih at 100-105 ⁰ C, the reaction mixture was cooled to ambient temperature. The reaction mixture was filtered over celite. The organic phase thus obtained was diluted with MTBE (80OmL) and washed three times with water (50OmL portions), dried over magnesium sulphate and concentrated. The resulting crude product was fractionally distilled with a Vigreux column (lmBar, 70-81 ⁰ C) to give a colourless oil (39.6g, gc purity 90%). The oil was chromatographed on a silica gel column with 7 % EtOAc in hexane as elution agent giving 3-(3-methylphenyl)butanal (12.5g, gc ρurity> 99% ; yield 36%).

Odour: green, watery /marine, aldehydic, marenil.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-rf) ppm: 1.31 (d, 3H); 2.34 (s, 3H); 2.70 (m, 2H); 3.32 (m, IH); 7.00-7.23 (m, 4H); 9.70 (t, IH).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 21.42 (q, 1C); 22.15 (q, 1C); 34.21 (d, 1C); 51.68 (t, 1C); 123.69 (d, 1C); 127.24 (d, 1C); 127.52 (d, 1C); 128.53 (d, 1C); 138.21 (s, 1C); 145.38 (s, 1C); 201.96 (d, 1C).

MS: m/z (relative intensity) 162 (M ⁺ , 71), 147 (33), 144 (13), 133 (8), 129 (14), 119 (100), 117 (37), 105 (76), 91 (61), 77 (21), 65 (16), 51 (9), 41 (13), 39 (13).

ii) 3 -(3 -methy Icy clohexyl)butan- 1 -ol

5% Ru/ Al ₂ O ₃ (500mg, 5% w/w) was charged into a 25mL autoclave vessel with 3-(3- methylphenyl)butanal (1Og, 61.6mmol). The mixture was vigorously stirred under a hydrogen atmosphere (65Bar) at 130 ⁰ C for 5.5h. The reaction mixture was filtered, rinsed with cyclohexane and concentrated. The resulting crude product was distilled via a bulb-to- bulb distillation (4.5mBar, 125-13O ⁰ C) to give 3-(3-methylcyclohexyl) butan-1-ol (8g, gc pur ity > 90 % ; yield 76 % ) .

Odour: floral, muguet, green, lilac, terpineol.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-^) ppm: 0.60-1.95 (m, 28H); 0.80-0.86 (m, 12H); 0.82 3.56-3.70 (m, 4H).

¹³ C NMR (101 MHz, CHLOROFORM-^) ppm: 16.06 (q, 2C); 22.99 (q, 1C); 23.02 (q, 1C); 26.43 (t, 1C); 26.53 (t, 1C); 28.03 (t, 1C); 29.86 (t, 1C); 32.91 (d, 1C); 33.00 (d, 1C); 34.38 (d, 1C); 34.43 (d, 1C); 35.43 (t, 2C); 37.01 (t, 1C); 37.05 (t, 1C); 37.43 (t, 1C); 39.30 (t, 1C); 42.65 (d, 2C); 61.52 (t, 2C).

MS: m/z (relative intensity) (no M ⁺ ), 152 (3), 137 (2), 124 (57), 110 (8), 97 (77), 96 (36), 95 (51), 81 (37), 69 (21), 67 (17), 55 (100), 41 (28).

iii) 3-(3-methyl)cyclohexylbutanal

A solution of Dess Martin periodinane (17.4g, 41mmol, l.leq) in dichloromethane (25OmL) was charged into a 2L three-necked round-bottom flask, equipped with a mechanical stirrer and a reflux condenser. 3-(3-methylcyclohexyl)butan-l-ol (6.4g, 38mmol) was added dropwise, followed by a mixture of water (740 L) in dichloromethane (74OmL) at ambient temperature over 1.5h. After stirring for 2h at ambient temperature, the mixture was diluted with diethyl ether (20OmL) and washed with a 1:1 mixture of saturated aqueous NaHCO ₃ and 10% Na ₂ S ₂ O ₃ (2xl00mL) and brine (10OmL), dried over magnesium sulphate and concentrated. The oil was chromatographed on a silica gel column with 7% EtOAc in hexane as elution agent giving 3-(3-methyl)cyclohexylbutanal (1.8g, gc purity > 80% ; yield 28%).

Odour: aldehydic, green, muguet.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 0.54-0.83 (m, 4H); 0.83-0.91 (m, 12H); 1.12-1.47 (m, 8H); 1.53-1.67 (m, 6H); 1.68-1.77 (m, 2H); 1.89-1.99 (m, 2H); 2.13-2.22 (m,2H); 2.40-2.48 (m, 2H); 9.73 (dd, 2H).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 16.87 (q, 2C); 22.92 (q, 1C); 22.93 (q, 1C); 26.25 (t, 1C); 26.32 (t, 1C); 28.57 (t, 1C); 29.68 (t, 1C); 32.78 (d, 1C); 32.87 (d, 1C); 33.00 (d, 1C); 33.02 (d, 1C); 35.21 (t, 2C); 37.91 (t, 1C); 39.01 (t, 1C); 42.55 (d, 1C); 42.56 (d, 1C); 48.50 (t, 1C); 48.51 (t, 1C); 203.46 (d, 2C).

MS: m/z (relative intensity) 168 (M ⁺ , < 1), 150 (2), 135 (11), 124 (75), 109 (10), 97 (49), ^' 95 (88), 81 (21), 71 (14), 69 (18), 68 (16), 67 (17), 55 (100), 41 (33).

Example 4 - Preparation of 3-(3-isopropylcyclohexyDbutanal

i) 2-[2~(3-isopropylphenyl)propyl]-l ,3-dioxolane

Ethylene glycol (18mL, 0.32mol, 1.2eq), paratoluene sulfonic acid (400mg, 1% w/w) and cyclohexane (5OmL) were charged into a IL three-necked round-bottom flask, equipped with a dean and stark, a reflux condenser and a mechanical stirrer. Florhydral™ 3-(3- isopropylphenyl)butanal, 49.3g, 0.26mol) was added dropwise at ambient temperature.- The stirred mixture was then heated for 3h at reflux. The reaction mixture was cooled at ambient temperature and washed water (2xl00mL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled with a Vigreux column (7.2mBar,

146°C), to give 2-[2-(3-isopropylphenyl)propyl]-l,3-dioxolane (239g, gc purity > 98% ; yield 97%).

Odour: floral.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 1.25 (d, 6H, J=7.08 Hz); 1.30 (d, 3H, J=7.08 Hz); 1.83-1.90 (m, IH); 1.98 - 2.04 (m, IH); 2.85-2.99 (m, 2H); 3.76-3.84 (m, 2H); 3.92-3.99 (m, 2H); 4.70 (dd, IH, J=6.35, 4.15 Hz); 7.02-7.08 (m, 3H); 7.20-7.25 (m, IH).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 22.63 (q, 1C); 24.03 (q, 2C); 34.11 (d, 1C); 36.02 (d, 1C); 42.10 (t, 1C); 64.62 (t, 1C); 64.75 (t, 1C); 103.35 (d, 1C); 124.02 (d, 1C); 124.21 (d, 1C); 125.25 (d, 1C); 128.29 (d, 1C); 146.64 (s, 1C); 148.93 (s, 1C).

MS: m/z (relative intensity) 234 (M ⁺ , 1), 190 (1), 172 (7), 157 (7), 148 (43), 133 (13),- 131 (13), 117 (10), 115 (12), 105 (100), 100 (1), 99 (20), 91 (22), 87 (46), 77 (8), 73 (93), 45 (22).

ii) 2-[2-(3-isopropylcyclohexyl)propyl]-l ,3-dioxolane

5% Ru/ Al ₂ O ₃ (2g, 5% w/w) was charged into a 10OmL autoclave vessel with 2-[2-(3- isopropylphenyl)propyl]-l,3-dioxolane (4Og, 0.17mol). The mixture was vigorously stirred under an hydrogen atmosphere (60-65Bar) at 13O ⁰ C for 4h. The reaction mixture was filtered, rinsed with cyclohexane and concentrated to give 2-[2-(3-

isopropylcyclohexyl)propyl]-l,3-dioxolane (126.5g, gc purity> 98%; yield> 99%) in the form of a colourless oil. The material was used as such for the next step.

Odour: green, pyraziαe, dusty, vetiver.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-^ ppm: 0.72 (dd, 2H, J= 16.24, 12.08 Hz); 0.83 (d, 6H, /=6.84 Hz); 0.82 (d, 6H, /=6.84 Hz); 0.89 (d, 3H, /=6.84 Hz); 0.88 (d, 3H, J=6.84 Hz); 0.92-1.82 (m, 26H); 3.78-3.85 (m, 4H); 3.91-3.98 (m, 4H); 4.87 (dd, 2H, /=5.62, 4.64 Hz).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 16.21 (q, 1C); 16.42 (q, 1C); 19.64 (q, 1C); 19.68 (q, 1C); 19.81 (q, 1C); 19.84 (q, 1C); 26.56 (t, 1C); 26.65 (t, 1C); 28.24 (t, 1C); 29.72 (t, 1C); 29.76 (t, 1C); 29.99 (t, 1C); 31.89 (t, 1C); 33.09 (d, 1C); 33.11 (d, 1C); 33.67 (t, 1C); 34.35 (d, 1C); 34.41 (d, 1C); 38.12 (t, 1C); 38.43 (t, 1C); 43.06 (d/ 1C); 43.20 (d, 1C); 44.19 (d, 1C); 44.27 (d, 1C); 64.57 (t, 1C); 64.58 (t, 1C); 64.74 (t,- 1C); 64.74 (t, 1C); 104.20 (d, 1C); 104.24 (d, 1C).

MS: Major isomer: m/z (relative intensity) (no M ⁺ ), 152 (2), 135 (1), 109 (3), 95 (2), 82 (4), 73 (100), 69 (4), 67 (5), 55 (5), 45 (7), 41 (6).

Minor isomer: m/z (relative intensity) (no M ⁺ ), 152 (2), 135 (1), 109 (3), 95 (2), 82 (4), 73 (100), 69 (4), 67 (5), 55 (5), 45 (7), 41 (7).

iii) 3-(3-isoρropylcyclohexyl)butanal

2-[2-(3-isopropylcyclohexyl)propyl]-l,3-dioxolane (5g, 20.8mmoi) and a 4:1 mixture of dichloromethane: acetone (30OmL) were charged into a 3L three-necked round-bottom flask equipped with a reflux condenser and a mechanical stirrer. Iron (HI) chloride hexahydrate (19.7g, 72.8mmol, 3.5eq) was added at ambient temperature. The reaction mixture was then stirred at ambient temperature for 4h and subsequently quenched at 5-1O ⁰ C with the addition of saturated aqueous NaHCO ₃ (50OmL). The organic phase was then washed with brine (50OmL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled via a Vigreux column (1.3mBar, 89 ⁰ C), to give 3-(3- isopropylcyclohexyl)butanal (23.9g, gc purity > 91%; yield 62%).

Odour: green, violet, orris, aldehydic.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-^) ppm: 0.65- 0.76 (m, 2H); 0.78-0.94 (m, 4H); 0.80-0.85 (m, 6H); 0.82 (d, 6H, J=6.84 Hz); 0.90 (d, 3H, J=7.08 Hz); 0.89 (d, 3H, J=6.84 Hz); 0.97-1.10 (m, 2H); 1.12-1.28 (m, 4H); 1.51-1.69 (m, 8H); 1.72-1.82 (m,- 2H); 1.90-2.02 (m, 2H); 2.13-2.23 (m, 2H); 2.42 (dd, IH, J=4.88, 1.71 Hz); 2.46 (dd, IH, J=4.88, 1.95 Hz); 9.73 (dd, 2H, J=2.81, 2.08 Hz).

¹³ C NMR (101 MHz, CHLOROFORM-^) ppm: 16.74 (q, 1C); 17.03 (q, 1C); 19.56 (q, 1C); 19.58 (q, 1C); 19.79 (q, 1C); 19.81 (q, 1C); 26.37 (t, 1C); 26.45 (t, 1C); 28.84 (d,- 1C); 29.46 (t, 1C); 29.51 (t, 1C); 29.96 (t, 1C); 32.64 (t, 1C); 33.01 (d, 1C); 33.02 (d, 1C); 33.16 (d, 2C); 33.66 (t, 1C); 42.73 (d, 1C); 42.83 (d, 1C); 44.01 (d, 1C); 44.10 (d, 1C); 48.39 (t, 1C); 48.64 (t, 1C); 203.36 (d, 1C); 203.40 (d, 1C).

MS: m/z (relative intensity) (no M ⁺ ), 178 (2), 163 (2), 152 (49), 135 (24), 125 (9), 123 (13), 109 (74), 95 (13), 93 (12), 82 (100), 69 (77), 67 (41), 55 (39), 41 (49).

Example 5 - Preparation of 3-(3-isopropylcyclohexyl)-2-memylbutanal

i) 3-(3-isopropylcyclohexyl)-2-metliylenebιιtanal

A solution of 3-(3-isopropylcyclohexyl)butanal (6g, 30.5mmol) in isopropanol (3.5mL) followed by formaldehyde (37% wt in water, 30.5mmol, leq) was charged into a 5OmL three-necked round-bottom flask equipped with a reflux condenser and a mechanical stirrer. Propionic acid (228 L, 3.0mmol, O.leq) and pyrrolidine (255 L, 3.0mmol, O. leq) were added at ambient temperature. The reaction mixture was then stirred at 45 ⁰ C for 3h; The crude mixture was cooled to ambient temperature dissolved in MTBE (10OmL) and washed with saturated aqueous NaHCO ₃ (10OmL), brine (10OmL), dried over magnesium sulphate and concentrated. The crude product was chromatographed on a silica gel column with 3 % EtOAc in hexane as elution agent giving 3-(3-isopropylcyclohexyl)-2- methylenebutanal (5g, gc purity > 99%; yield 78 %) .

Odour: woody, fruity, green, aldehydic.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 0.48-1.82 (m, 40H), 2.50-2.63 (m, 2H), 5.98-6.03 (m, 2H), 6.17-6.22 (m, 2H), 9.48 - 9.53 (m, 2H).

¹³ C NMR (101 MHz, CHLOROFORM-^ ppm: 15.87 (q, 1C), 16.08 (q, 1C), 19.49 (q, 2C), 19.85 (q, 2C), 26.32 (t, 1C), 26.40 (t, 1C), 29.10 (t, 1C), 29.27 (t, 1C), 29.29 (t,. 1C), 31.28 (t, 1C), 32.77 (t, 1C), 32.99 (d, 1C), 33.07 (d, 1C), 34.82 (t, 1C), 36.72 (d, 1C), 36.75 (d, 1C), 41.40 (d, 1C), 41.62 (d, 1C), 43.88 (d, 1C), 44.00 (d, 1C), 133.97 (t, 2C), 154.69 (s, 1C), 154.73 (s, 1C), 194.78 (d, 1C), 194.80 (d, 1C).

MS: Minor isomer: m/z (relative intensity) 208 (M ⁺ , 1), 193 (1), 165 (3), 147 (7), 125 (62), 109 (5), 105 (4), 95 (5), 91 (6), 83 (47), 69 (100), 55 (35), 41 (33).

Minor intensity m/z (relative intensity): 208 (M ⁺ , 1), 193 (1), 165 (2), 147 (5), 125 (63), 109 (4), 105 (4), 95 (4), 91 (5), 83 (47), 69 (100), 55 (33), 41 (31).

ii) 3-(3-isopropylcyclohexyl)-2-methylbutanal

5% Pd/C (250mg, 5% w/w) was charged into a 25mL autoclave vessel with 3-(3- isopropylcyclohexyl)-2-methylenebutanal (4.5g, 21.6mmol) in methanol (5mL). The mixture was vigorously stirred under an hydrogen atmosphere (lOBar) at 40-45° C for 40 minutes. The catalyst was filtered over celite and the solution was concentrated. The resulting crude product was distilled with a bulb-to-bulb distillation (2.5mBar, 117°C) to- give 3-(3-isopropylcyclohexyl)-2-methylbutanal (3g, gc purity > 90% ; yield = 67%).

Odour: green, violet, apple, cucumber.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 0.57-0.79 (m, 2H), 0.79-0.93 (m, 18H), 0.95 (dd, 2H, J=6.96, 2.81 Hz), 1.01-1.05 (m, 6H), 1.06-1.31 (m, 4H), 1.31-1.46 (m, 5H), 1.46-1.70 (m, 8H), 1.70-1.86 (m, 3H), 2.27-2.56 (m, 2H), 9.60-9.64 (m, 2H).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 11.67 (q, 1C), 11.70 (q, 1C), 13.95 (q, 1C), 14.05 (q, 1C), 19.51 (q, 1C), 19.62 (q, 1C), 19.80 (q, 1C), 19.83 (q, 1C), 26.39 (t, 1C), 26.58 (t, 1C), 28.03 (t, 1C), 29.37 (t, 1C), 29.52 (t, 1C), 31.73 (t, 1C), 31.80 (t, 1C), 33.00 (d, 1C), 33.03 (d, 1C), 35.30 (t, 1C), 39.26 (d, 1C), 39.42 (d, 1C), 39.76 (d,

1C), 39.77 (d, 1C), 44.01 (d, 1C), 44.30 (d, 1C), 49.69 (d, 1C), 49.82 (d, 1C), 206.04 (d, 1C), 206.09 (d, 1C). .

MS: Major isomer: m/z (relative intensity) 210 (M ⁺ , < 1), 192 (1), 177 (2), 152 (48), 149 (14), 123 (12), 109 (66), 97 (14), 95 (15), 82 (100), 69 (82), 55 (47), 41 (49).

Example 6 - Preparation of 3-(3-fert-butvlcvclohexvDbutanal

i) 3-(3-tert-butylphenyl)butanal

In a IL three-necked round-bottom flask equipped with a mechanical stirrer and a reflux condenser were introduced DMF (20OmL), l-bromo-3-tert-butylbenzene (54.3g, 0.25mol), crotyl alcohol (65mL, 0.76mol, 3eq), sodium carbonate (66.2g, 0.62mol, 2.5eq), tetrabutyl ammonium bromide (69.5g, 0.25mol, leq), palladium acetate (5.05g, 7.5mmol, 3mol%) and tri-o-tolyl phosphine (7.6g, 25mmol, O.leq). After stirring for Ih at 90- 100 ⁰ C, the reaction mixture was cooled toambient temperature. The reaction mixture was filtered over celite. The organic phase thus obtained was diluted with MTBE (50OmL) and washed three times with water (50OmL portions), dried over magnesium sulphate and concentrated. The resulting crude product was distilled with a bulb-to-bulb distillation (3mBar, 121 ⁰ C) to give a colourless oil (34.7g, gc purity 73%). The crude product was chromatographed on a silica gel column with 5% EtOAc in hexane as elution agent giving 3-(3-fert-butylρhenyl)butanal (12.3g, gc purity 99%; yield 39%).

Odour: floral, aldehydic, muguet, marine.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 1.33 (d, 3H, J=5.86 Hz); 1.32 (s, 9H); 2.61-2.80 (m, 2H); 3.36 (qt, IH, J=7.16, 6.96 Hz); 7.01-7.07 (m, IH); 7.23-7.27 (m, 3H); 9.72 (t, IH, /=2.08 Hz).

¹³ C NMR (101 MHz, CHLOROFORM-^) ppm: 22.15 (q, 1C); 31.35 (q, 3C); 34.53 (d, 1C); 34.66 (s, 1C); 51.83 (t, 1C); 123.49 (d, 1C); 123.55 (d, 1C); 123.91 (d, 1C); 128.30 (d, 1C); 145.06 (s, 1C); 151.48 (s, 1C); 202.04 (d, 1C).

MS: m/z (relative intensity) 204 (M ⁺ , 12), 189 (31), 171 (4), 161 (30), 147 (100), 145 (81), 130 (17), 119 (24), 117 (23), 115 (21), 105 (25), 91 (36), 77 (14), 65 (8), 57 (52), 41 (31).

ii) 3-(3-tert-butylcyclohexyl)butan-l-ol

5% Ru/ Al ₂ O ₃ (75mg, 5% w/w) was charged into a 25mL autoclave vessel with 3-(3-tert~ butylphenyl)butanal (1.5g, 52mmol). The mixture was vigorously stirred under an hydrogen atmosphere (60-65Bar) at 13O ⁰ C for 1Oh. The reaction mixture was filtered, rinsed with cyclohexane and concentrated. The resulting crude product was distilled with a bulb-to-bulb distillation (0.5mBar, 125-135 ⁰ C) to give 3-(3-te??-butylcyclohexyl)butan-l-ol (Ig, gc purity > 99%; yield 62%).

Odour: odourless.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-^) ppm: 0.63-0.80 (m, 2H); 0.81-0.87 (m, 6H); 0.83 (s, 18H); 0.87-1.88 (m, 26H); 3.54-3.80 (m, 4H).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 15.91 (q, 1C); 16.35 (q, 1C); 26.84 (t, 1C); 26.93 (t, 1C); 27.50 (t, 1C); 27.51 (t, 1C); 27.57 (q, 3C); 27.58 (q, 3C); 28.08 (t, 1C); 29.72 (t, 1C); 29.93 (t, 1C); 31.57 (t, 1C); 32.54 (s, 1C); 32.57 (s, 1C); 34.70 (d, 1C); 34.71 (d, 1C); 36.85 (t, 1C); 37.40 (t, 1C); 43.08 (d, 1C); 43.31 (d, 1C); .48.27 (d, 1C); 48.35 (d, 1C); 61.65 (t, 1C); 61.73 (t, 1C).

MS: Minor isomer: m/z (relative intensity) (no M ⁺ ), 197 (1), 194 (2), 179 (1), 166 (23), 155 (30), 137 (30), 123 (11), 110 (43), 109 (41), 95 (62), 83 (35), 81 (94), 69 (44), 67 (48), 57 (100), 41 (56).

Major isomer: m/z (relative intensity) (no M ⁺ ), 197 (1), 194 (2), 179 (1), 166 (26), 155 (35), 137 (34), 123 (13), 110 (46), 109 (44), 95 (64), 83 (36), 81 (97), 69 (45), 67 (49), 57 (100), 41 (56).

iii) 3-(3-ter^butylcyclohexyl)butanal

A solution of Dess Martin periodinane (1.8g, 4.2mmol, l. leq) in dichloromethane (3OmL) was charged into a 25OmL three-necked round-bottom flask, equipped with a mechanical stirrer and a reflux condenser. 3-(3-te7t-butylcyclohexyl)butan-l-ol (805mg, 3.79mmol) was added dropwise, followed by a mixture of water (75 L) in dichloromethane (75mL) at ambient temperature, over 1.5h. After stirring for 2h at ambient temperature, the mixture was diluted with diethyl ether (10OmL) and washed with a 1: 1 mixture of saturated aqueousNaHCO ₃ and 10% aqueous Na ₂ S ₂ O ₃ (5OmL) and brine (5OmL). The organic phase was dried over magnesium sulphate and concentrated. The crude product was

chromatographed on a silica gel column with 5% EtOAc in hexane as ehition agent giving 3-(3-tert-butylcyclohexyl)butanal (lOOmg, gc purity > 93 %; yield 13%).

Odour: aldehydic, floral, herbal, watery.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 0.60-1.95 (m, 20H); 0.82 (s, 18H); 0.89- 0.92 (t, 6H); 1.93 (m, 2H); 2.15-2.47 (m, 4H); 9.74 (m, 2H).

13C NMR (101 MHz, CHLOROFORM-d) ppm: 16.67 (q, 1C); 17.19 (q, 1C); 26.63 (t, 1C); 26.71 (t, 1C); 27.34 (t, 2C); 27.54 (q, 6C); 28.61 (t, 1C); 29.75 (t, 1C); 30.34 (t/ 1C); 31.33 (t, 1C); 32.54 (s, 1C); 32.55 (s, 1C); 33.28 (d, 1C); 33.31 (d, 1C); 43.01 (d, 1C); 43.16 (d, 1C); 48.11 (d, 1C); 48.18 (d, 1C); 48.33 (t, 1C); 48.78 (t, 1C); 203.44 (s, 1C); 203.50 (s, 1C).

MS: Minor isomer: m/z (relative intensity): (no M ⁺ ), 177 (4), 166 (19), 135 (26), 121 (8), ^' 109 (54), 95 (23), 93 (15), 81 (37), 79 (22), 67 (42), 57 (76), 55 (38), 41 (100), 39 (49).

Major isomer: m/z (relative intensity): (no M ⁺ ), 177 (4), 166 (19), 135 (26), 121 (8), 109 (46), 95 (22), 93 (14), 81 (33), 79 (19), 67 (40), 57 (68), 55 (31), 41 (100), 39 (45).

Example 7 - Preparation of 2-memyl-3-f3-memylcvclohexyr)ρropanal

i) (2£)-2-memyl-3-(3-memylρhenyl)acrylaldehyde

A solution of potassium hydroxide (24g, 0.36mol, 0.6eq, with a purity of 85%) in ethylene glycol (12Og) and water (12g) was charged into a 50OmL three-necked round-bottom flask equipped with a reflux condenser and a mechanical stirrer. 3-methyl benzaldehyde (7Og, 0.59mol) was added dropwise. The stirred reaction mixture was heated at 38-42 ⁰ C and propionaldehyde (41g, 0.71mol, 1.2eq) was dosed in over 3.25h. After a further hour at 40 ⁰ C, the reaction mixture was cooled to ambient temperature and the two layers separated. The organic layer thus obtained was washed with water (2xl00mL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled via a Vigreux column (l.OmBar, 87-92 ⁰ C), to give (2£)-2-methyl-3-(3- methylphenyl)acrylaldehyde (65.9g, gc purity > 95% ; yield 70%).

Odour: spicy, cinnamon.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 2.09 (d, 3H); 2.42 (s, 3H); 7.20-7.38 (m, 5H); 9.59 (s, IH).

¹³ C NMR (101 MHz, CHLOROFORM-^) ppm: 10.92 (q, 1C); 21.37 (q, 1C); 127.08 (d, 1C); 128.54 (d, 1C); 130.33 (d, 1C); 130.70 (d, 1C); 135.05 (s, 1C); 138.13 (s, 1C); 138.31 (s, 1C); 150.03 (d, 1C); 195.55 (d, 1C).

MS: m/z (relative intensity): 160 (M ⁺ , 25), 159 (22), 145 (100), 131 (12), 128 (14), 117 (60), 115 (60), 105 (5), 91 (42), 77 (13), 65 (13), 63 (14), 51 (14), 39 (25).

ii) 2-methyl-3-(3-memylcyclohexyl)propan-l-ol

5% Ru/ Al ₂ O ₃ (630mg, 2.7% w/w) was charged into a 5OmL autoclave vessel with (2E)-2- methyl-3-(3-methylphenyl)acrylaldehyde (23.5g, 0.15mol). The mixture was vigorously stirred under an hydrogen atmosphere (45-50Bar) at 160 ⁰ C for 7h. The catalyst was filtered and the solution was rinsed with cyclohexane and concentrated. The resulting crude product was distilled via a Vigreux column (5mBar, 102-104 ⁰ C) to give 2-methyl-3-(3- methylcyclohexyl)propan-l-ol (13.7g, gc purity > 81 % ; yield 60%).

Odour: floral, muguet, citrus.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-^) ppm: 0.4-1.8 (m, 28H); 0.83-0.90 (m, 12H); 3.32-3.35 (m, 4H).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 16.84 (q, 1C); 16.845(q, 1C); 22.92 (q, 1C); 22.94 (q, 1C); 26.26 (t, 1C); 26.34 (t, 1C); 32.58 (d, 1C); 32.60 (d, 1C); 32.62 (d/ 1C); 32.72 (d, 1C); 33.84 (t, 2C); 34.79 (d, 1C); 34.81 (d, 1C); 35.32 (t, 2C); 41.19 (t, 1C); 41.21 (t, 1C); 41.96 (t, 1C); 43.16 (t, 1C); 68.73 (t, 1C); 68.74 (t, 1C).

MS: Major isomer: m/z (relative intensity) (no M ⁺ ), 152 (7), 137 (7), 123 (5), 110 (41), 97 (46), 95 (100), 82 (44), 81 (52), 69 (32), 67 (24), 55 (97), 41 (34).

Minor isomer: m/z (relative intensity) (no M ⁺ ), 152 (5), 137 (6), 123 (5), 110 (39), 97 (35), 95 (100), 82 (43), 81 (53), 69 (29), 67 (24), 55 (89), 41 (34).

iii) 2-methyl-3-(3-methylcycloliexyl)ρropanal

A solution of Dess Martin periodinane (4.1g, 9.7mmol, l.leq) in dichloromethane (43mL) was charged into a 25OmL three-necked round-bottom flask, equipped with a mechanical stirrer and a reflux condenser. 2-methyl-3-(3-methylcyclohexyl)propan-l-ol (1.5g, 8.8mmol) was added dropwise, followed by a mixture of water (127 L) in dichloromethane (127mL) at ambient temperature, over Ih. After stirring for Ih at ambient temperature, the mixture was diluted with diethyl ether (10OmL) and washed with a 1:1 mixture of saturated aqueous NaHCO ₃ and 10% aqueous Na ₂ S ₂ O ₃ (5OmL) and brine (5OmL), dried over, magnesium sulphate and concentrated. The crude product was chromatographed on a silica gel column with 5 % EtOAc in hexane as elution agent giving 2-methyl-3-(3- niethylcyclohexyl)propanal (800mg, gc purity > 90% ; yield 54%).

Odour: floral, citrus, cuminic, nitrile.

Analytical data (2 isomers):

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 0.4-1.8 (m, 24H); 0.84 (d, 6H); 1.04 (d, 6H); 2.30-2.60 (m, 2H); 9.56 (d, 2H).

¹³ C NMR (101 MHz, CHLOROFORM-d) ppm: 13.74 (q, 1C); 13.76 (q, 1C); 22.81 (q, 1C); 22.83 (q, 1C); 26.08 (t, 1C); 26.13 (q, 1C); 32.52 (d, 2C); 32.57 (t, 1C); 33.22 (t, 1C); 34.99 (d, 1C); 35.02 (d, 1C); 35.12 (t, 1C); 35.17 (t, 1C); 38.31 (t, 1C); 38.35 (t, 1C); 41.85 (t, 1C); 42.49 (t, 1C); 43.72 (d, 1C); 43.74 (d, 1C); 205.58 (s, 2C).

MS: Major isomer: m/z (relative intensity) 168 (M ⁺ , 1), 150 (5), 135 (10), 125 (6), 111 (68), 110 (58), 97 (26), 95 (63), 83 (17), 82 (22), 81 (27), 69 (59), 67 (22), 58 (36), 55 (100), 41 (41).

Minor isomer: m/z (relative intensity) 168 (M ⁺ , < 1), 150 (3), 135 (12), 125 (5), 110 (60), 97 (22), 95 (75), 83 (15), 82 (26), 81 (32), 69 (63), 67 (26), 58 (40), 55 (100), 41 (45).

Example 8 - Preparation of 2,2-dimethyl-3-(3-methylcγclohexyl)propanal

i) 2,2-dimethyl-3-(3-methylcyclohexyl)propan-l-ol

5% Rh/C (450mg, 15% w/w) was charged into a 5OmL autoclave vessel containing a mixture of 2,2-dimethyl-3-(3-methylplienyl)propan-l-ol (6g, 34mmol) in water (17mL). The mixture was vigorously stirred under an hydrogen atmosphere (lOBar) at 60 ⁰ C for 6h. The reaction mixture was filtered and the filtrate was extracted with MTBE (25mL), dried over magnesium sulphate and concentrated. The resulting crude product was distilled with a bulb-to-bulb distillation (2.5mBar, 90 ⁰ C) to give 2,2-dimethyl-3-(3- methylcyclohexyl)propan-l-ol (5.1g, gc purity > 99%; yield 82%).

Odour: aldehydic, fatty /greasy, floral.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-d) ppm: 0.51-0.88 (m, 2H), 0.79-0.87 (m, 9H), 0.95-1.76 (m, 10H), 1.87 (br. s., IH), 3.25 (s, 2H).

¹³ C NMR (101 MHz, CHLOROFORM-^ ppm: 22.90 (q, 1C), 24.30 (q, 1C), 24.31 (t, 1C), 26.53 (d, 1C), 32.90 (d, 1C), 33.58 (t, 1C), 34.83 (t, 1C), 35.48 (t, 1C), 35.68 (s, 1C), 44.95 (t, 1C), 46.26 (t, 1C), 72.32 (t, 1C).

MS: Major isomer: m/z (relative intensity) (no M ⁺ ), 153 (34), 137 (3), 111 (11), 97 (100), 83 (29), 69 (20), 55 (74), 41 (23).

Minor isomer m/z (relative intensity): (no M ⁺ ), 153 (33), 137 (6), 111 (11), 97 (100), 83 (30), 69 (23), 55 (79), 41 (25).

ii) 2,2-dimethyl-3-(3-methylcyclohexyl)propanal

A solution of Dess Martin periodinane (9.Og, 21.lmm.ol, 1.3eq) in dichloromethane (165mL) was charged into a 25OmL three-necked round-bottom flask, equipped with a mechanical stirrer and a reflux condenser. The solution was cooled to 0 ⁰ C by the mean of an ice/salt bath. 2,2-dimethyl-3-(3-methylcyclohexyl)propan-l-ol (3.0g, 16.3mmoi) was added dropwise. After stirring for 2h at ambient temperature, the mixture was cooled down to -15 ⁰ C and the solid was filtered off. The organic solution was then concentrated. The resultant crude product was chromatographed on a silica gel column with 2% EtOAc in hexane as elution agent giving 2,2-dimethyl-3-(3-methylcyclohexyl)propanal (1.Og, gc purity > 85 % ; yield 33 %) .

Odour: marine, watery.

Analytical data:

¹ H NMR (400 MHz, CHLOROFORM-^) ppm: 0.45-0.79 (m, 2H), 0.81 (d, 3H, J=6.59 Hz), 1.02 (s, 6H), 1.10-1.79 (m, 10H), 9.45 (t, IH).

¹³ C NMR (101 MHz, CHLOROFORM-^) ppm: 21.98 (q, 1C), 22.09 (q, 1C), 22.81 (q, 1C), 26.22 (t, 1C), 32.66 (d, 1C), 34.13 (t, 1C), 34.20 (d, 1C), 34.77 (t, 1C), 43.47 (t, 1C), 45.78 (t, 1C), 45.94 (s, 1C), 206.80 (d, 1C).

MS: Major isomer: m/z (relative intensity) 182 (M ⁺ , < 1), 164 (2), 153 (15), 135 (2), 125 (4), 111 (21), 97 (100), 83 (28), 72 (94), 69 (30), 55 (89), 41 (32).

Example 9 - Odour Intensity

3-(3-tert-butylcyclohexyl)propanal, hereafter referred to as Compound 1, was diluted in DPG to a level of 10 wt%. For comparison a 10 wt% solution in DPG of Florhydral™, and a neat Lily aldehyde™ composition were prepared.

The three compositions were added to a smelling strip and the odour intensity was assessed by a number of professional perfumers. All the perfumers indicated that the Compound 1 had a more intense odour than the Lily aldehyde™ and Florhydral™.

Example 10 - Performance on hair

Pantene™ shampoo was dosed at 0.2% - 80mg of ingredient was added to 4Og of Pantene™ shampoo base. Pantene™ shampoo dosed with 0.2% Lily aldehyde™ was used as the standard (scale 0 to 10; Lily aldehyde™ = 5). Unperfumed Pantene™ was used for the control.

"Caucasian European" origin switches were used. Switches were wetted and 10% by weight of the dry hair switch was added in product. The shampoo was massaged in to the hair switch for 30s. The muguet odour intensity (foaming intensity) was then assessed. The switches were rinsed under hand hot warm water and towel dried. The muguet odour intensity (damp intensity) was then assessed. The hair switches were line dried for 3 hours in an odour free room. The muguet odour intensity (dry intensity) was then assessed.

Compound 1 outperformed Florhydral™ in Pantene™ shampoo. It showed very linear performance on foaming, damp and dry hair and proved much more substantive on dry hair than any of the benchmarks.

Example 11 - Performance in Ariel high suds (handwash powder)

Ariel™ high suds were dosed at 0.1 % - 20mg of ingredient were added to 2Og of powder. Ariel™ high suds dosed with 0.1 % Lily aldehyde™ was used as the standard. Unperfumed Ariel™ high suds was used for the control.

The bloom from bowl was assessed by dissolving 4.5g of Ariel™ high suds in 2 litres of tepid water, in a plastic bowl. Two terry towelling cloths were stirred in the solution for 5- minutes. The wash solution was assessed (scale 0 to 10; Lily aldehyde™ = 5), giving the intensity from bowls figure. One cloth was rinsed in tepid water, hand wringed and odour assessed for rinsed cloth intensity (scale as above).

Ariel™ high suds containing Compound 1 showed greater intensity than Florhydral™. Rinsed cloth with Ariel™ high suds containing Compound 1 outperformed the benchmarks, indicating good substantivity on cloth.

Example 12 - Performance in Candle Wax

Candle wax house base (IGI hard paraffin wax mix) was dosed at 1.0% - candles were left to mature at room temperature for 24 hours before assessment. All ingredients were used as 10% dilutions in benzyl benzoate. Intensity was assessed, by a panel of perfumers, from candle placed in fragrance booths for one hour. AU candles were first evaluated in the cold wax before burning. Candles were then burned for one hour, in the fragrance booth, and odour assessed again for the bum mode intensity.

Compound 1 was much stronger than all of the benchmarks, both in cold wax and in burn- mode.

Example 13 - Insect Repellencv

Results

Compound 1 was tested for insect repellency against mosquitoes and ants. In all cases, repellency is calculated with reference to an untreated surface having 0% repellency.

Tests results showed an excellent repellency against mosquitoes (100% repellency after 10 minutes, wrt untreated surface).

Compound 1 showed very good activity against ants (72% repellency over first hour, wrt untreated surface).

Protocols:

Ant test is completed with a simplified general purpose cleaner formulation:

Synperonic 91-6 5.0%

Perfume . ingredient 1.0%

Water 94.0%

This product is applied to the floor tiles (vinyl) at the rate of 2Og. m ^"2 .

Ant (Lasius niger)

300mm square vinyl tiles half treated with 0.9ml test material and left for 2 hours.

Glass arena 250mm square, 75mm high and fluon coated, open to air.

Arena illuminated from 1.0m above by four 18W fluorescent lamps.

50 black ants per arena counted every 5 minutes.

Arena turned 180 degrees every 10 minutes.

Any ants injured or escaping replaced.

Mosquito (Aedes aegyptii)

A perspex box approx 18 inch cube, with sleeved circular entry was used as the test cage.

The box contained 5 day old, mated honey fed females.

The area of arm to be tested was measured.

The test material was applied from ethanol solution at a rate of 0.2mg test material per square centimetre.

A similar area of the other arm was used for the control.

A pair of disposable gloves was worn on the hands throughout the test.

In turn each arm was inserted into the cage for 30 seconds. This was repeated 3 times.

The number of mosquitoes landing on the arm was recorded every five seconds.

As penetration of the skin occurs within 5 seconds the arm was flicked at this frequency to dislodge the flies.

Example 14 - Antimicrobial

Minimum Inhibitory Concentration (MIC)

One property that characterises the effectiveness of a compound or composition to inhibit the growth of bacteria, is the rnήήmum inhibitory concentration, or MIC, of the compound or composition. The MIC is defined as the rninimum amount of a compound or composition (e.g. hi ppm) at which little or no bacterial growth is observed. Generally, the lower the MIC of a compound or composition for a bacterium, the more effective the compound will be at inMbiting bacterial growth.

The minimum inhibitory concentration of a compound was determined by the following method.

A culture of the test strains of bacteria Staphylococcus aureus ATCC 6538 (American Type Culture Collection, P.O. Box 1549, Manassas, VA20108, USA) was incubated for 16-24 hours, in a shaken flask at 37°C. The cultures was then diluted in sterile 0.1 % TSB (Oxoid, Basingstoke, UK) to give a concentration of bacteria of approximately 10 ⁶ colony forming units (cfu) per ml.

Fragrance compounds were prepared hi sterile TSB to give stock solutions with final concentrations of 40,000 ppm. The absorbance at 540nm (hereinafter referred to for brevity and simplicity as "A ₅₄₀ ") was used as a measure of turbidity resulting from bacterial growth. The MIC was taken as the concentration of ingredient required to inhibit growth so that the average change hi absorbance during the incubation period was < 0.2

The results are shown below.

Example 15 -Malodour Counteracting:

Fragrance materials were tested using small-scale tabletop method (3mL malodour in 15mL jar + ImL material oil in 15mL jar both placed in 50OmL jar (where either fragrance or malodour is tested alone DEP should be placed in the other 15mL jar). Bathroom malodour is used at 0.5%.

The perceived intensity of malodour and fragrance in each jar is assessed by a trained sensory panel using a line scale anchored at the extremes (0 — 100). The malodour control is- used as a standard (perceived intensity 75) against which all other perceived intensities are scaled.

A further jar was prepared as "hidden controls", also containing malodour only, but the panellists are unaware that it does not contain a fragranced, or active, product.

Compounds 3 and 4 were tested for malodour counteracting performance when at 1% w/w in DPG. They significantly reduced the perceived intensity of malodour and have similar performance as Cyprisate™ and Camonal™, which are well-known malodour counteractants.

Example 16 - Perfumed Products

A perfuming composition for a water based gel air freshener was prepared by admixing the following ingredients:

¹ l-(2-((3-methylbutyl)oxy)ethyl)benzene; origin: Quest International, UK.

² l-(2-((l-(emyloxy)ethyl)oxy)ethyl)benzene; origin: Quest International, UK.

³ 3-((l-ethyloxy)ethyl)oxy)-3,7-dimethyl-l,6-octadiene; origin: Quest International, UK. ⁴ 3a,4,5,6,7,7a-hexahydro-4,7-methano-lH-inden-6-yl proρanoate; origin: Quest International, UK.

⁵ 4-methyl-2-(2-methylpropyl)tetrahydro-2H-4-pyranol: Quest International, UK.

⁶ ethyl S-isopropylbicycloP^.ljhept-S-ene^-carboxylate; origin: Quest International, UK.

⁷ tricyclo[5.2.1.0 2,6]dec-4-en-8-yl ethanoate; origin: Quest International, UK.

⁸ 2-hexylcyclopentan-l-one; origin: Quest International, UK.

⁹ cis and trans 2,4-dimethyl-3-cyclohexene-l-carbaldehyde; origin: Quest International, UK.

¹⁰ methyl 2-(3-oxo-2-ρentylcyclopentyl)ethanoate; origin: Quest International, UK. ¹¹ 2-(l,l-dimethylethyl)cyclohexyl ethanoate; origin: Quest International, UK. ¹² 3,6-dihydro-4,6-dimethyl-2-phenyl-2H-pyran; origin: Quest International, UK.

¹³ mixture of oxacycloheptadecan-2-one and cyclopentadecanone; origin: Quest International, UK.

¹⁴ compounded perfumery base; origin: Quest International, UK.

The addition of 0.25 % of Compound 1 to the above-described perfuming composition, instead of an equivalent amount of Dihydro Myrcenol, enhanced the perceived odour intensity of the fragrance and imparted freshness, white/floralcy to the composition.

A perfuming composition for a general purpose cleaner was prepared by admixing the following ingredients:

* in dipropyleneglycol

¹ 4-tricyclo(5.2.1.0 2,6)dec-8-ylidenbutanal; origin: Quest International, UK.

² l-(2-((l-(ethyloxy)ethyl)oxy)ethyl)benzene; origin: Quest International, UK.

³ 3-((l-ethyloxy)ethyl)oxy)-3,7-dimethyl-l,6-octadiene; origin: Quest International, UK.

⁴ 4-methyl-2-(2-methylpropyl)tetrahydro-2H-4-pyranol: Quest International, UK.

⁵ 2-hexylcyclopentan-l-one; origin: Quest International, UK.

⁶ 3-methyl-5-phenylpentanol; origin: Quest International, UK.

⁷ methyl 2-(3-oxo-2-pentylcyclopentyl)ethanoate; origin: Quest International, UK.

The addition of 0.50% of Compound 1 to the above-described perfuming composition, instead of an equivalent amount of Linalol, enhanced the perceived odour intensity of the fragrance and imparted freshness, white/floralcy to the composition.