Mixtures of dimethyl-tricyclo (5.2.1.02,6) decane derivatives together with their preparation and use as a scent-and flavor materials

Abstract

Mixtures of new dimethyl-tricyclo[5.2.1.0.sup.2,6 ]decane derivatives, notably the primary isomers of the common formula A, whereinR.sup.1 and R.sup.2 mean either methyl group or hydrogen, one of the substituents being a methyl group and the other hydrogen,R.sup.3 and R.sup.4 mean either methyl group or hydrogen, one of the substituents being a methyl group and the other hydrogen, andX indicates the .pi.-system of a C-C double bond or an epoxide system, can advantageously be used as new acent- and flavor materials.The compounds of the common formula A, were prepared by hydrogenation of dimeric methylcyclopentadiene selectively in the norbornane part and when desired by epoxidation of the remaining double bond. ##STR1##

Description

Description

Dicyclopentadiene (1) is an important starting material for scent production. Ester 2b-c obtained by the addition of carboxylic acids (e.g. acetic acid, propionic acid) are used for scents worldwide in large amounts (preparation: Zeilanov et al., Chem. Abstracts 68, 49319d). The format 2a is described in U.K. Pat. No. 815,232 (24.6.1959) and the dimethylacrylate 2d in U.S. Pat. No. 3,593,745 (10.8.1971). Further products from dicyclopentadiene were comprehensively described by Ohloff and Rode-Gawal (in: H. Aebi, E. Baumgartner, H. P Fiedler and G. Ohloff, "Kosmetika, Riechstoffe und Lebensmittelzusatzstoffe"; G. Thieme Verlag, Stuttgart 1978, pp. 55-57). ##STR2##

Little is known about the products of dimeric methylcyclopentadiene (3). In European patent application No. 0 039 232 were claimed as scents dimethyltricyclodecane derivatives of the common formula 4 obtained from dimeric methyl cyclopentadiene 3, the broken line representing an optional double bond. The methyl group in the norbornane part should alternatively be contained in the R.sub.1 or R.sub.2 group and the methyl group in the cyclopentene part should alternatively be contained in the R.sub.4, R.sub.5 or R.sub.6 group. The respective non-substituted positions R.sub.1, R.sub.2, R.sub.4-6 should be occupied by hydrogen. The molecular group Y should be a carbonyl--, hydroxyl--, acetate--, propionate--, or a C.sub.3 -- or C.sub.4 -- ether group. The products consist of isomeric mixtures.

Compounds of the common formula 5 were claimed in German patent specification No. 1 218 643 (6.6. 1966), possessing perfume properties. ##STR3##

German OLS 3 120 700 A1 (25.2.1982) described tricyclodecane derivatives of the common formula 6 and their use as scents.

The present invention relates to a mixture of new dimethyltricyclo[5.2.1.0.sup.2,6 ]decane derivatives, notably primary isomers of the common formula A ##STR4## R.sup.1 and R.sup.2 mean either methyl group or hydrogen, one of the substituents being a methyl group and the other hydrogen,

R.sup.3 and R.sup.4 mean either methyl group or hydrogen, one of the substituents being a methyl group and the other hydrogen, and X indicates the .pi.-system of a c--c double bond or an epoxide system.

Methylcyclopentadiene [preparation: review in W. T. Ford, J. Org. Chem. 25, 3979 (1971)] exists as a mixture of three double-bonded isomers 3a,b,c. According to S. McLean and P. Haynes, (Tetrahedron, 21, 2313 (1965)) it exists in equilibrium as 44.5% of 1-methyl-isomer 3a, 54.5% of C-2-isomer 3b and only about 1% of C-5-isomer 3c.

By the dimerisation of an equilibrium mixture of methylcyclopentadiene a plurality of products can theoretically be prepared. Under the hypothesis, that products with angular methyl groups are sterially unfavourable and do not arise in significant amounts, and that the product derived from 3c (<1%) can be ignored, the dimeric methylcyclopentadiene ##STR5## (gas chromatogram: FIG. 1) should consist of the structural isomers 7a-f. The .sup.1 H-NMR spectrum (FIG. 2) indicates signal groups in the range of olefinic protons (5-6 ppm) which correspond to their integral 2,2 protons. The signals at 1.25 and 1.50 ppm can by analogy with dicyclopentadiene (Sadtler NMR Spectra Collection No. 6494M) be classified as the protons of the C.sub.1 -bridge. Only the relatively low-intensity signals of 1.23 and 1.35 ppm can be classified as the bridging methyl group of 7a-c. These findings and the intensities of the olefinic signals point to the preponderant presence of isomer 7d-f (about 85%), while 7a-c exists as only about 15%. ##STR6##

The selective hydrogenation of the norbornane part of the dimethylcyclopentadiene isomers 7a-f is achieved by modification of that of Ch. A. Brown for the selective hydrogenation of dicyclopentadiene (1) given in the review [Ch. A. Brown, Chem. Commun. 1969, 952; H. C. Brown and Ch. A. Brown, J. Am. Chem. Soc., 85, 1004 (1963)]. Using nickel boride producted in situ hydrogenation was done in methanol, ethanol, or another polar, aprotic solvent at temperatures of 20.degree.-80.degree. C., preferably at 40.degree.-50.degree. C., and a hydrogen pressure of 30-70 bar, preferably 50-60 bar. The thus-obtained new mono-enes 8a-f exist according to the gas chromatagram (FIG. 3) as a mixture of the three primary isomers (approx. 16, 24 and 37%) together with secondary isomers, that as 7a-f can be treated as structural isomers but also as stereo isomers. All these isomers show a very similar mass spectrometric breakdown pattern which can be explained by the opening of the norbornane system by formation of methylcyclopentadienyl radicals cation (m/z 80) and a methylcyclopentane (typical mass spectrum: FIG. 7). In the .sup.1 H-NMR spectrum (FIG. 4) are the characteristic signals for olefinic protons of .delta.=5.1-5.3 ppm (1 H) and those for olefinic methyl groups of 1.7 ppm of the cyclopentene system with tri-substituted double bond. Singlets at 1.25 and 1.15 ppm can identify bridging methyl groups of the isomers 8a-c and two superposed doublets at 1.05 ppm the methyl groups of the norbornane part of the isomers 8d-f, that exist as primary isomers.

The mixture of mono-enes 8a-f obtained by hydrogenation of 7a-f possess a strong smell of fresh-green, herblike ##STR7## character. A solution of the mono-enes 8a-f in sugar syrup (10%) at a concentration of about 2 g/100 kg had an interesting taste tending towards aniseed and eucalyptus.

A mixture of new epoxides 9a-f was obtained by epoxidation of 8a-f. The epoxidation was carried out in known per ser manner with peracetic acid, whereby a polar, inert solvent, preferably methylene chloride or chloroform was added together with a neutralizing material, preferably sodium acetate or sodium carbonate. The mixture of new epoxides 9a-f obtained from 8a-f consists according to the gas chromatagram (FIG. 5) of three primary components (a: 15%, b: 44%, c: 32%) and a few secondary components. The three primary components show distinct mass spectrometric fragmentation behaviour (FIGS. 8, 9, 10). In the .sup.1 H-NMR-spectrum (FIG. 6) the abovementioned epoxide system was characterised by the signals for the oxirane proton at .delta.=3.0-3.2 ppm and the singlet of the methyl group at .delta.=1.40 ppm. The remaining methyl group signals appear analogous to 8a-f. The primary isomers should therefore possess the structures 9d-f.

The epoxide mixture 9a-f possesses a strong, fresh-herblike smell that is reminiscent of cedarleaf oil and clary sage oil. The taste of a solution of 9a-f in 10% sugar syrup at a concentration of 1 g/100 kg would be described as woody-earthy and sweet.

Because of their smell- and taste-properties the new dimethyltricyclodecane derivatives 8a-f, 9a-f (common formula A) can be used as scent- and flavour materials. This will be demonstrated by the following use examples.

EXAMPLE 1

Preparation of dimethyl-tricyclo[5.2.1.0.sup.2,6 ]decenes 8a-f

150 ml of an ethanolic 1 m NaBH.sub.4 -- solution were dropped while stirring into a mixture of 139.5 g (0.56 mol). Ni(Ac).sub.2.4H.sub.2 O and 1.9 l ethanol in an atmosphere of nitrogen (15 min). This precipitated nickel boride as a fine-grained, black deposit. After addition of 1.44 kg (9 mol) of dimeric methylcyclopentadiene the nitrogen atmosphere was evacuated. Hydrogenation followed for 16 hours at a pressure of 50-60 bar and a temperature of 40.degree.-50.degree. C. After filtration, concentration and distillation 2.57 kg (88%) 8a-f was obtained as a colourless oil; bp (2.67 mbar)=76.degree.-82.degree. C.; density d=0.9417; refraction: n=1.4989. Gas chromatogram: FIG. 3, .sup.1 H-NMR: FIG. 4, MS: FIG. 7. C.sub.12 H.sub.18 (162.4).

EXAMPLE 2

Preparation of dimethyl-tricyclo[5.2.1.0.sup.2,6 ]decane-epoxide 9a-f

A washing of 1060 g Na.sub.2 CO.sub.3 in 970 g (6 mol) 8a-f (according to Example 1) and 3 l CHCl.sub.3 was added with 1.9 kg peracetic acid (40% in acetic acid) at 40.degree. C. (slight cooling) for 2.5 hours. After stirring for 10 hours at room temperature 100 ml of water were added. Concentration and distillation over a 30 cm Vigreux column gave 970 g (90%) of 9a-f as a colourless oil; bp (1.35 mbar)=85.degree.-100.degree. C.;

density: d=1.0230; refraction: n=1.4944. GC: FIG. 5, .sup.1 H-NMR: FIG. 6, MS: FIGS. 8, 9, 10. C.sub.12 H.sub.18 O (178.5)

EXAMPLE 3

Perfume oil with herb-like character

______________________________________ (a) (b)______________________________________Cedar-leaf oil 150 --epoxide 9a-f -- 150oil of bergamot 100 100phenylethyl alcohol 100 100terpinol 100 100acetylcedrene 100 100amyl salicylate 70 70linalyl acetate 60 60benzyl salicylate 50 50cumarine 50 504-tert-butylcyclohexylacetate 50 50anisaldehyde 50 50gamma methylionone 50 50linanool 50 50Tunisian oil of rosemary 45 45Brahmanol .RTM. (2,2,3-trimethylcyclopent-3-ene- 40 403'-methyl-4'-hydroxy-butyl-)oil of citronella 30 30ylang-ylang oil 30 30attractolide (ethylenedioxo-dodecandioate) 30 30oil of spike (lavender) 20 20clary sage oil 10 10geranium oil 5 5Brasillian oil of peppermint 5 5galbanum extract 5 5 1200 1200______________________________________

The perfume oil of mixture a possesses a herblike-fresh fragrance. By the exchange of the epoxide 9a-f for the cedarleaf oil a new sweet-herblike fragrance is obtained, which distinguishes itself by strong emission and cohesiveness.

EXAMPLE 4

Perfume base with green character

______________________________________ (a) (b)______________________________________benzyl salicylate 200 200.alpha.-hexyl-cinnamaldehyde 200 200linalylacetate 200 200methyldihydrojasmonate 100 100oil of basil 80 80storax extract 20 20oil of wormwood 10 10citral 10 10dimethytricyclodecene 8a-f -- 70dipropylene glycol 170 110 1000 1000______________________________________

The perfume base of mixture a has a measurable green-fruity fragrance. The addition of the mono-ene 8a-f (mixture b) adds a fresh head character and a sweet-herblike secondary character, so that mixture b has a natural effect.

EXAMPLE 5

Perfume oil-base of "chrysanthemum-green" type

______________________________________epoxide 9a-f 100linanool 70isoeugenol-methylether 50campholene aldehyde 50mandarin oil 50oil of buchu, 1% in diproylene glycol 50Paraguayan oil of petitgrain 40.beta.-ionone 30oil of basil 20helional 20allyl-phenoxyacetate 10indole, 10% in diproylene glycol 10 500______________________________________

The perfume oil, which contains a large amount of 9a-f, possesses a measurable sharp-green fragrance which is reminiscent of chrysanthemum leaves.

Claims

1. Mixtures of dimethyl-tricyclo[5.2.1.0.sup.2,6 ]decane derivatives which comprise isomers of the formula ##STR8## wherein R.sup.1 and R.sup.2 are either methyl or hydrogen with the proviso that R.sup.1 and R.sup.2 must be different; R.sup.3 and R.sup.4 are either methyl or hydrogen with the proviso that they must be different.

2. A perfumed composition which consists of an odor imparting quantity of a compound of claim 1.