1,2,6-Trimethyltricyclo[5,3,2,0.sup.2,7 ]dodeca-5-one perfume composition

Abstract

1,2,6-Trimethyltricyclo[5,3,2,0.sup.2,7 ]dodeca-5-one having the formula (I) ##SPC1##and a process for producing this compound. This compound is useful as a perfume.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to a tricyclic hydrocarbon, 1,2,6-trimethyltricyclo[ 5,3,2,0.sup.2,7 ]dodeca-5-one, and to a process for producing this tricyclic hydrocarbon compound.

2. Description of the Prior Art

Amber-like fragrant substances are important starting materials for a blended perfume, and of these substances, ambergris obtainable from sperm whales is the most expensive. The fragrance component of ambergris was clarified by E. Laderer and L. Ruzicka in 1946 to be a substance formed from ambrein which is a triterpene compound. Ever since, many attempts to synthesize amber-like fragrant substances equal to the natural material, or similar substances have been made. Some of them can be utilized as a substitute for expensive ambergris. For example, manool derivatives, which are diterepene compounds and can be obtained from a special needle-leaf tree, are widely used as such a substitute. However, in general, amber-like fragrant substances are difficult to synthesize and moreover, special natural products are requried as a starting material to synthesize amber-like fragrant substances. Therefore, synthetic amber-like fragrant substances are inevitably expensive.

SUMMARY OF THE INVENTION

This invention provides 1,2,6-trimethyltricyclo-[5,3,2,0.sup.2,7 ]dodeca-5-one having the formula ##SPC2##

And a process for producing 1,2,6-trimethyltricyclo[5,3,2,0.sup.2,7 ]-dodeca-5-one (hereinafter "Compound (I)") comprising isomerizing 5,6-epoxy-1,2,6-trimethyltricyclo[5,3,2,0.sup.2,7 ]dodecane (hereinafter referred to as "Compound (II)") with a Lewis acid.

BRIEF DESCRIPTION OF THE ACCOMPANYING DRAWINGS

FIG. 1 is an infrared spectrum of Compound (I) obtained according to the present invention.

FIG. 2 is a mass spectrum of Compound (I) obtained according to the present invention.

FIG. 3 is an NMR spectrum of Compound (I) obtained according to the present invention.

FIG. 4 shows the stereostructural form of a ketone compound obtained by isomerization of Compound (I).

DETAILED DESCRIPTION OF THE INVENTION

Compound (I) produced according to the present invention is a sesquiterpene compound having the molecular formula, C.sub. 15 H.sub. 24 O, and a structure represented by the formula (I) ##SPC3##

According to this invention, Compound (I) can be obtained much more cheaply than conventional amber-like fragrant substances, and is also of industrial value because of its excellent amber-like fragrance.

According to the present invention, Compound (I) can be prepared by adding Compound (II) dropwise to a mixed solution of a Lewis acid such as AlX.sub. 3, ZnX.sub.2 and MgX.sub.2 (wherein X is Cl, Br. or I) or a boron trifluoride-diethyl ether complex salt, etc. and a solvent inert to the Lewis acid, e.g., ethers such as diethyl ether, dipropyl ether, etc., hydrocrbons such as n-hexane, n-octane, benzene, toluene, etc., halogenated hydro-carbons such as dicholormethane, chloroform, etc., esters such as ethyl acetate, butyl acetate, etc., and the like, at a temperature of about -10.degree. to 30.degree.C, and isomerizing Compound (II) with the Lewis acid. Alternatively the reaction can be conducted in the absence of an inert solvent but the reaction proceeds more smoothly when an inert solvent is employed.

When the boron trifluoride-diethyl ether complex salt is used as a Lewis acid, a suitable amount thereof is about 1/20 to 1/30 mole per mole of Compound (II). Further, when other Lewis acids are used, a suitable amount thereof is about 0.1 to 1.2 moles per mole of Compound (II), with 1 mole being preferred to achieve an isomerization which proceeds most smoothly and in which better results are obtained. A preferred isomerization temperture is 5.degree. to 10.degree.C. When the isomerization temperature exceeds about 30.degree.C, a large amount of polymeric materials are formed. The isomerization is sensitive to moisture and, thus anhydrous conditions are employed and the isomerization is preferably carried out in a dry air or a dry nitrogen atmosphere. A sufficient isomerization time in the preferred isomerization temperture range as described above is about 4 to 5 hours. After completion of the isomerization, the resulting solution is acidified, i.e., with cold dilute hydrochloric acid, dilute sulfuric acid, etc., and then extracted with a solvent such as diethyl ether, benzene, etc. Subsequently, the extract is distilled in vacuo, whereby crystalline Compound (I) can be obtained in a yield of 75% or more.

Compound (II) used as a starting material in the process of this invention can be produced by subjecting 1,5,9-trimethylcyclododecatrine-1,5,9 (hereinafter 1,5,9-TMCDT), which is a cyclic trimer of isoprene to an intramolecular ring closure reaction with an acid catalyst to form 1,2,6-trimethyltricyclo-[5,3,2,0.sup.2,7] dodeca-5-ene (hereinafter "Compound (III)"), and treating this compound with a peracid. The intramolecular ring closure reaction and the reaction with the peracid are, respectively, disclosed in copending US patent applications Ser. No. 537,004, filed Dec. 27, 1974, (corresponding to Japanese Patent Application Nos. 4207/1974 and 102646/74) and Ser. No. 537,039, filed Dec. 27, 1974, (corresponding to Japanese Patent Application No. 6388/1974) both filed simultaneously herewith.

Compound (I) is a fragrant substance having a rich natural ambergris-like fragrance, a peculiar wood-like odor, a camphor-like diffusibility and a so called "natural odor" reminiscent of moist earth or a sunshiney forest. When Compound (I) is absorbed on filter paper, and allowed to stand in a room at room temperture, (e.g., about 20.degree..gtoreq.30.degree.C) the residual fragrance is very strong and lasts for over 1 week. The fragrant odor of Compound (I) also is strong and even when Compound (I) is diluted with ethyl alcohol, the average person even can perceive Compound (I) even at a one-tenthousandth dilution.

The utility value and application range of Compound (I) of this invention are wide as a perfumery material. That is, Compound (I) can be widely used as a perfume, for example, as a component for a rich perfume to a perfume for a relatively inexpensive soap, by utilizing its residual fragrance and economy. It is possible to use Compound (I) together with rich natural amber, or musk civet, or as a substitute therefor by utilizing its ambergris-like fragrance, or together with natural sandalwood oil, vetiver oil, patchouli oil, cedar oil, etc., or as a substitute therefor by utilizing its wood-like fragrance, thereby providing a dry and rough scent necessary for a man's perfume.

Now, the present invention will be described in detail, by reference to the following Reference Example, Examples and drawings. The examples are merely illustrative and are not to be construed as limiting the scope of the present invention. Unless otherwise indicated, all parts, percents, ratios and the like are by weight.

REFERENCE EXAMPLE

i. Process for Preparing 1,2,6-trimethyltricyclo[5,3,2,0.sup.2,7 ]-dodeca-5-ene, Compound (III), from 1,5,9-trimethylcyclododecatriene-1,5,9, 1,5,9-TMCDT:

Into a 1l three-necked flask were charged 150 g of 1,5,9-trimethylcyclododecatriene-1,5,9 (melting point: 91.degree. -92.degree. C), 260 ml of formic acid and 150 ml of dichloromethane, and the materials were mixed. The mixture was kept at a temperature of 5.degree. to 10.degree.C. Then, a mixture of 7.5 ml of sulfuric acid and 40 ml of formic acid was added dropwise thereto over a period of 30 minutes, while keeping the temperature at 5.degree. to 10.degree.C. Subsequently, the materials were reacted with stirring at that temperature for 3 hours, and further reacted with stirring at room temperature (i.e., about 20.degree.-30.degree.C) for 3 additional hours. After completion of the reaction, dichloromethane was recovered by distillation, and formic acid was then distilled off under reduced pressure. The residue was neutralized and washed with a 3% aqueous sodium bicarbonate solution, washed with water, and dried with anhydrous sodium sulfate. Then, the residue was distilled in vacuum, whereby 135 g of the frction of 1,2,6-trimethyltricyclo-[5,3,2,0.sup.2,7 ]dodeca-5-ene (75.degree.-80.degree.C/0.05 mmHg) was obtained.

ii. Process for Preparing Compound (II) from 1,2,6-trimethyltricyclo]5,3,2,0.sup.2,7 ]dodeca-5-ene, Compound (III):

A mixture of 20.4 g (0.1 mole) of 1,2,6-trimethyltricyclo[5,3,2,0.sup.2,7 ]dodeca-5-ene and 17 g of sodium carbonate was added to 100 ml of dichloromethane, and the materils were mixed and stirred while keeping the temperature at 0.degree. to 5.degree.C. Then, 20.8 g (0.11 mole) of an acetic acid solution containing 40% peracetic acid was added dropwise thereto over a period of 2 hours at that temperature. The materials were stirred at that temperature for 2 hours, and further stirred at room temperature for 3 additional hours. Subsequently, 200 ml of water was added thereto, and the resulting solution was extracted twice with dichloromethane. The extract was washed with an aqueous saturated sodium chloride solution until the solution became neutral, and then dried with anhydrous sodium sulfate. Dichloromethane was then recovered by distillation, and the residue was distilled in vacuum, whereby 21 g of the fraction of Compound (II) (85.degree.-90.degree.C/0.03 mmHg) was obtained.

EXAMPLE 1

13.4 g (0.1 mole) of AlCl.sub.3 and 100 ml of n-hexane were mixed under a dry nitrogen atmosphere, and the mixture was kept at 0.degree. to 10.degree.C. 22 g (0.1 mole) of Compound (II) was added dropwise thereto over a period of 1 hour. The materials were stirred at that temperature for 1 hour, and further stirred at room temperature for 2 additional hours. Then, the reaction solution was poured into 100 ml of cold dilute hydrochloric acid (6N), and the solution was extracted with n-hexane. The extract was dried with anhydrous sodium sulfate, and n-hexane was then distilled off. Subsequently, the residue was distilled in vacuum, whereby 20 g of the fraction (105.degree.-110.degree.C/0.05 mmHg) corresonding to Compound (I) was obtained. By recrystallizing this compound from methanol, 17.6 g of prism-like crystalline Compound (I) having a melting point of 99.5.degree. to 100.5.degree.C was obtained in a yield of 80%.

______________________________________Elemental Analysis: C HCalculated (%): 81.76 10.98Found (%): 81.75 10.98IR Spectrum: 1710 cm.sup..sup.-1 (.nu. C=0)MAS Spectrum: M.sup.+ 220 (molecular ion) M.sup.+--CH.sub.3 205 M.sup.+--CO 192NMR Spectrum: ##STR1## (a)0.95ppm(3H,s) (b)1.20ppm(3H,s) (c)0.89ppm(3H,d,J=7c ps) (d)2.77ppm(1H,q,J=7cps) (e)2.37ppm(2H,m)X-ray Crystal Structural Analysis (direct method):Lattice constant: a=7.975A, b=13.225A, c=7.147A .alpha.=95.7.degree., .beta.=60.0.degree., .gamma.=104.2.degree.Space group: P1, Z=2Values (A) of X, Y and Z as solid coordinates:Atom RX RY RZ______________________________________C1 0.9791 5.7703 1.7584C2 2.3424 5.6967 2.4672C3 3.1955 4.4961 2.0121C4 2.3586 3.2151 1.9691C5 3.0098 1.9672 1.2955C6 3.6074 2.3334 -0.0927C7 2.4712 2.8519 -1.0345C8 1.5720 3.8637 -0.3559C9 1.1293 3.4170 1.0436 C10 0.2013 4.4893 1.6283 C11 0.5477 1.9829 0.9738 C12 1.7833 1.0214 1.1082 C13 -1.1340 4.7008 0.8295 C14 1.9438 2.8689 3.4240 C15 4.1078 1.2928 2.165701 0.5492 6.8548 1.4110______________________________________ Bonding angle among atoms from the solid coordinates: ______________________________________Three Atoms Bonding Angle______________________________________ (degree)C2-C1-C10 117.21C1-C2-C3 113.06C3-C4-C9 109.94C5-C4-C14 109.74C4-C5-C12 102.04C6-C5-C15 109.29C6-C7-C8 112.52C4-C9-C10 110.05C8-C9-C11 109.68C1-C10-C13 111.65C5-C12-C11 104.92C2-C1-O1 119.15C2-C3-C4 110.94C3-C4-C14 107.85C9-C4-C14 112.11C4-C5-C15 113.57C12-C5-C15 111.06C7-C8-C9 112.68C4-C9-C11 101.76C10-C9-C11 115.93C9-C10-C13 114.50C10-C1-O1 123.46C3-C4-C5 116.95C5-C4-C9 100.20C4-C5-C6 110.94C6-C5-C12 109.74C5-C6-C7 109.65C4-C9-C8 110.69C8-C9-C10 108.58C1-C10-C9 108.39C9-C11-C12 105.50______________________________________

The stereostructural formula shown in FIG. 4 can be derived from the foregoing values.

Molecular Formula: C.sub.15 H.sub.24 O

From the foregoing results, Compound (I) was determined to have the following stereostructural formula (III) ##SPC4##

EXAMPLE 2

The reaction was carried out under the same conditions as described in Example 1, except that 0.57 g (0.004 moles) of boron trifluoride-diethyl ether complex salt was used in place of 13.4 g (0.1 mole) of AlCl.sub.3, whereby 17.2 g of Compound (I) was obtained in a yield of 78%.

EXAMPLE 3

The following formulation is suitable as a base for a perfume or an eau-de-cologne.

______________________________________ g______________________________________Civet Absolute 10Musk Absolute 5Oak Moth Absolute 30Vanilla Absolute 10Musk Ambrette 80Sandalwood Oil 50Patchouli Oil 80Methyl Ionone 30Vetiver Oil 100Eugenol 20Phenylethyl Alcohol 30Geraniol 30Benzyl Acetate 30Jasmine Absolute 20Hexylcinnamic Aldehyde 50Linalool 50Linalyl Acetate 50Bergamot Oil 125Compound (I) 50 850g______________________________________

EXAMPLE 4

The following formulation is suitable for a soap perfumery.

______________________________________ g______________________________________Ethylene Brassylate 90Sandalwood Oil 50Oakmoth Resinoid 10Patchouli Oil 50Coumarin 30Bornyl Acetate 15Citronellol 60Tetrahydrogeraniol 5Petigrain Oil 30Lavandine Oil 80Stearyl Acetate 15Pineneedle Oil 10Linalool 185Linalyl Acetate 120Compound (I) 50 800g______________________________________

While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.

Claims

1. A perfume composition containing 1,2,6-trimethyltricyclo[5,3,2,0.sup.2,7 ] dodeca-5-one having the formula (I) ##SPC5##

and other perfume ingredients.