US3751500A

US3751500A - Hydrogenated indane derivatives and processes for producing same

Info

Publication number: US3751500A
Application number: US00115834A
Authority: US
Inventors: J Hall
Original assignee: International Flavors and Fragrances Inc
Current assignee: International Flavors and Fragrances Inc
Priority date: 1969-08-18
Filing date: 1971-02-16
Publication date: 1973-08-07
Anticipated expiration: 1990-08-07

Abstract

A HYDROGENATED INDANE DERIVATIVE HAVING THE FORMULA:

1,1,2,3,3-PENTA(-)INDAN

WHEREIN THE DASHED LINES REPRESENT SINGLE OR DOUBLE BONDS, NO MORE THAN TWO OF THE DASHED LINES REPRESENT DOUBLE BONDS AND, WHEN TWO DOUBLE BONDS ARE PRESENT, SUCH BONDS BEING UNCONGJUGATED; PERFUME COMPOSITIONS CONTAINING SUCH INDANES; AND PROCESS FOR PRODUCING SAME.

Description

United States Patent 3,751,500 HYDROGENATED INDANE DERIVATIVES AND PROCESSES FOR PRODUCING SAME John B. Hall, Rumson, N.J., assignor to International Flavors & Fragrances Inc., New York, N.Y.

No Drawing. Original application Aug. 18, 1969, Ser. No. 851,086, now Patent No. 3,636,176. Divided and this application Feb. 16, 1971, Ser. No. 115,834

Int. Cl. C07c 13/46 US. Cl. 260-666 PY 6 Claims ABSTRACT OF THE DISCLOSURE A hydrogenated indane derivative having the formula:

wherein the dashed lines represent single or double bonds, no more than two of the dashed lines represent double bonds and, when two double bonds are present, such bonds being unconjugated; perfume compositions containing such indanes; and processes for producing same.

This application is a division of applicants copending parent application Ser. No. 851,086 filed on Aug. 18, 1969, now US. Pat. No. 3,636,176.

BACKGROUND OF THE INVENTION There is a continuing need for fragrance materials having persistent amber Woody odors with satisfactory overtones or qualities. While many natural products have amber woody fragrances, the more desirable of these are frequently in short supply and hence diflicult to obtain and expensive. Moreover, it is also most desirable that such amber woody fragrance character have good persistence so that the substances can be used in quality formulations for perfume or other olfactory compositions. Such materials should also possess good blending qualities so that they are useful in preparing perfume compositions.

THE INVENTION Briefly, the present invention provides a novel hydrogenated indane derivative, 4,5-dihydro-1,l,2,3,3-pentamethylindane, having the formula:

This substance has a strong, persistent, woody amber odor with various elegant piney overtones. Thus the present invention also provides novel perfume and fragrance compositions containing such hydrogenated indane, and processes for producing such indane are also disclosed herein.

The invention also contemplates 5,7a-dihydro1,1,2,3,3- pentamethylindane having the formula:

Patented Aug. 7, 1973 and 3a,4-dihydro-1,1,2,3,3-pentamethylindane having the formula:

and hexahydro-l,1,2,3,3-pentamethylindane having the formula:

These materials are useful in preparing a varietyof perfume compositions, as taught hereinafter.

It will be appreciated by those skilled in the art from the present disclosure that the indane derivatives according to this invention can exist in several stereoisomeric forms, and it is contemplated that the formula given herein includes the several isomeric forms.

A convenient starting material according to the present invention is pentamethylindane. In one aspect, the pentamethylindane is hydrogenated to provide the tetrahydro derivative and/or the hexahydro derivative as the first step in the synthesis. In this synthesis the bridge double bond of the tetrahydro derivative is then oxidized with a suitable agent to obtain the epoxyiudane.

The hexahydro derivative can be dehydrogenated if desired to obtain the 1,1,2,3,3 -pentamethylindane for recycling or for other syntheses. Such dehydrogenation can also provide a useful fragrance material.

For the tetrahydro derivative, the hydrogenation is carried out under controlled conditions to add two moles of hydrogen to each mole of the indane. It is preferred to use metallic catalysts such as Raney nickel or noble metals such as palladium, rhodium, and the like. Such catalysts can be supported on carriers such as carbon and the like.

The hydrogenation is carried out at substantially superatmospheric pressures of from 50 to 200 atmospheres, and is preferably carried out at 60 to atmospheres. The reaction is desirably carried out at temperatures in excess of 100 C. up to 225 C., and a preferred temperature range is to l90 C. The hexahydro derivative is obtained under these same conditions through the addition of three moles of hydrogen.

In one aspect, the 4,5,6,7-tetrahydropentamethylindane so obtained is oxidized to provide the epoxy oxygen substituent on the 3a, 7a bridge carbon atoms. The oxidation is carried out with an oxidizer such as percarboxylic acid. Thus, peracids such as peracetic, perpropionic, perbenzoic, perphthalic, and the like are used. In preferred embodiments of the process, lower aliphatic percarboxylic acids are used. Thus, peracetic acid can be used, although a combination of acetic anhydride and hydrogen peroxide is equivalent. The amount of percarboxylic acid used should be about stoichiometric, although slight excesses up to about ten molar percent can be used. An alkali metal salt of the corresponding carboxylic acid, e.g., sodium acetate for peracetic acid, is desirably used to buifer the reaction mixture.

The dihydropentamethylindane is formed by refluxing the epoxide as prepared above with sulfuric acid or a sulfonic acid agent such as benzenesulfonic acid, p-toluenesulfonic acid, methanesulfonic acid, and the like or a Lewis acid such as boron trifluoride, boron trifluorideetherate, and the like. Such agent is present in catalytic amounts.

This reaction can be carried out at pressures above or below atmospheric, but atmospheric pressure is desired to minimize ebullition of any reaction vehicle and provide an acceptable reaction rate, while maintaining control over the reaction. The temperatures used are in the range of 15 to 120 C., depending upon the catalyst used.

The reaction is suitably carried out in the presence of a vehicle, and solvents for the epoxide and agent are desirable. Such reaction vehicles include aromatic hydrocarbons such as benzene, toluene, xylene, and the like, and benzene is a preferred vehicle.

Other dihydro derivatives can be produced directly from the pentamethylindane or by isomerization of the 4, S-dihydro derivative described above. Thus, the pentamethylindane can be treated with an alkali metal, desirably lithium, in liquid or gaseous ammonia also to provide the 5,7a-dihydro derivatives. Such treatment is carried out at temperatures of from about -40 C. to about 25 C. At the lower temperature atmospheric or slightly subatmospheric pressures can be used. With liquid am monia at the higher temperatures, superatmospheric pressures up to about five atmospheres are used. Reaction times of from 15 minutes to four hours can be used.

The conjugated 3a, 4 dihydro derivative is produced from the non-conjugated material by treatment with an alkali metal, preferably lithium, in an alkylamine, desirably a lower alkylamine such as ethylamine and the like. While it can be conducted at subor superatmospheric pressures, the reaction is desirably carried out at atmospheric pressures. Temperatures of to 17 C. are used, and the time is from 30 minutes to four hours.

The hydrocarbons produced according to the above reaction schemes can be separated from the vehicle and any unreacted materials or unwanted by-products removed by conventional means including washing, distillation, extraction, preparative chromatography, and the like. It is preferred to fractionally distill the washed reaction product under a relatively high vacuum so as to obtain a pure product. Product purities of 80% are readily obtained, and much higher purities can also be provided by suitable treatment. All parts, proportions, percentages and ratios herein are by weight unless otherwise indicated.

The dihydropentamethylindanes of this invention are useful as fragrances. They can be used to contribute a woody amber fragrance. As olfactory agents the indane derivatives of this invention can be formulated into or used as components of a perfume composition.

The term perfume composition is used herein to mean a mixture of organic compounds, including, for example, alcohols, aldehydes, ketones, esters, and frequently hydrocarbons which are admixed so that the combined odors of the individual components produce a pleasant or desired fragrance. Such perfume compoistions usually contain: (a) the main note or the bouquet or foundationstone of the composition; (b) modifiers which round-off and accompany the main note; (0) fixatives which include odorous substances which lend a particular note to the perfume throughout all stages of evaporation, and sub stances which retard evaporation; and (d) top-notes which are usually low-boiling fresh-smelling materials.

In perfume compositions the individual component will contribute its particular olfactory characteristics, but the overall eflect of the perfume composition will be the sum of the effect of each ingredient. Thus, the individual compounds of this invention, or mixtures thereof, can be used to alter the aroma characteristics of a perfume composi tion, for example, by highlighting or moderating the olfactory reaction contributed by another ingredient in the composition.

The amount of the compounds of this invention which will be effective in perfume compositions depends on many factors, including the other ingredients, their amounts and the effects which are desired. It has been found that perfume compositions containing as little as 2% by weight of the compounds of this invention, or even less, can be used to impart a woody amber odor to soaps, cosmetics, and other products. The amount employed can range up to 7% or higher and will depend on considerations of cost, nature of the end product, the effect desired on the finished product and the particular fragrance sought.

The indane derivatives of this invention can be alone or in a perfume composition as an olfactory component in determgents and soaps; space deodorants; perfumes; colognes; bath preparations such as bath oil and bath salts; hair preparations such as lacquers, brilliantines, pomades, and shampoos; cosmetic preparations such as creams, deodorants, hand lotions, and sun screens; powders such as talcs, dusting powders, face powder, and the like. When used as an olfactory component of a perfumed article, as little as 0.011% of the novel hydrocarbon will suifice to impart a fine woody amber odor.

In addition, the perfume composition can contain a vehicle or carrier for the other ingredients. The vehicle can be a liquid such as alcohol, glycol, or the like. The carrier can be an absorbent solid such as a gum or components for encapsulating the composition.

It will be appreciated that the pentamethylindane derivatives according to this invention can be used to enhance, modify, or supplement the fragrance properties of natural or synthetic fragrance compositions. Thus, such preferred dihydroindanes can be used in fragrance compositions for addition to perfume compositions or directly to products such as soap, detergents, cosmetics, and the like. The fragrance compositions so prepared do not entirely provide the olfactory properties to the finished perfume or other article, but they do furnish a substantial part of the overall fragrance impression.

The following examples are given to illustrate embodiments of the invention as it is presently preferred to practice it. It will be understood that these examples are illustrative, and the invention is not to be considered as re stricted thereto except as indicated in the appended claims.

EXAMPLE I Preparation of 4,5,6,7 tetrahydro-1,1,2,3,3-pentamethylindane and hexahydro-l,l,2,3,3-pentamethylindane The following ingredients are charged into a stainless steel five-liter autoclave equipped with a hydrogen gas feed: 1,800 g. (8.14 moles) of l,1,2,3,3-pentamethylindane pure), and g. of Raney nickel.

Enough hydrogen is fed into the autoclave to raise the pressure to 1,000 p.s.i.g. The hydrogen feed is continuous until two moles of hydrogen are absorbed, and the autoclave is heated to a temperature in the range of C. over a period of about 8 hours until an amount of H equal to 10% in excess of theory is absorbed. During this time the pressure in the autoclave is maintained at 1,500 p.s.i.g.

The 1,641 g. of crude product removed from the autoclave is distilled on a 12-inch Goodloe column after being mixed with 10.0 g. of Primol mineral oil. The distillate is recovered in two fractions.

Fraction I: Distills at a temperature of 80 C. and 4.0 mm. Hg to provide 401 g. of 4,5,6,7-tetrahydro-1,1,2, 3,3-pentamethylindane.

Fraction II: Distills at a temperature range of 86- 88 C. and 3.5-3.8 mm. Hg to provide 729 grams of hexahydro- 1, 1,2,3,3-p entamethylindane.

A sample of Fraction I is further refined on a six-foot by Az-inch gas liquid chromatographic (GLC) column containing 20% Carbowax polyethylene glycol and operated at 110 C. Analysis by infrared (IR) and proton magnetic resonance PMR) confirms the structure:

Fraction II is further refined in a similar manner and analysis confirms the structure:

EXAMPLE II (a) Production of 3a,7a-epoxyhexahydro-1,1,2,3,3-

pentamethylindane Into a 250 ml. flask equipped with thermometer, stirrer, reflux condenser and ice bath are introduced 194 g. of the tetrahydroindane produced in Example I and 15 g. of sodium acetate. At 25-30 C., 124 g. of 40% peracetic acid (0.65 mole) is added during four hours. After addition is completed, an equal volume of water is added to the reaction mass. The aqueous phase is separated from the organic phase and extracted with 150 ml. of toluene. The toluene extract is combined with the organic phase and washed with one volume of 5% aqueous sodium hydroxide solution and then with one volume of water.

The solvent is stripped ofl leaving a crude product weighing 208 g. The crude epoxy product is distilled on a 12-inch Goodloe column after addition of 4.0 g. of triethanolamine at 72-74 C. and 1.0-1.4 mm. Hg. PMR and IR analysis of this material confirm the structure:

(b) Production of 4,5-dihydro-1,1,2,3,3-pentamethylindane Into a 100 ml. reaction flask fitted with thermometer and reflux condenser are introduced 10 g. of the epoxyhexahydroindane produced above, 50 ml. benzene, and 0.5 g. of p-toluenesulfonic acid. The reaction mass is stirred for two hours at 2030 C. and then refluxed for one hour.

The reaction mass is subsequently washed with a saturated aqueous sodium bicarbonate solution followed by one volume of a sodium chloride solution and dried over anhydrous sodium sulfate. The resulting product is separated on a gas-liquid chromatographic (GLC) column and the various separated constituents are analyzed by PMR, mass, infrared and UV absorption spectroscopy. These analyses confirm the identity of 4,5-dihydro-1,1,2, 3,3-pentamethylindane having the structure:

This material has a fine woody, amber-tobacco aroma with an elegant piney note.

6 EXAMPLE n1 Preparation of soap composition A total of g. of soap chips (from a toilet soap prepared from tallow and coconut oil) is mixed with one gram of the perfume composition given below until a sub stantially homogeneous composition is obtained. The soap composition manifests a characteristic woody-amber odor with piney overtones.

The perfume composition comprises the following ingradients:

EXAMPLE 1V Preparation of a detergent composition A total of 100 grams of a detergent powder is mixed with 0.15 gram of the perfume composition as set forth in Example III until a substantially homogeneous composition having a Woody-amber odor is obtained.

EXAMPLE V Preparation of a cosmetic powder composition A cosmetic powder is prepared by mixing 100 grams of talcum powder with 0.25 gram of the dihydroindane obtained from the process of Example II in a ball mill. The cosmetic powder has a desirable Woody-amber odor.

EXAMPLE VI Liquid detergent Concentrated liquid detergents with a woody-amber, piney odor are prepared containing 0.1%, 0. 15%, and 0.20% of the dihydroindane produced in Example II. They are prepared by adding and homogeneously mixing the appropriate quantity of the compound to Ultra Chemical Companys P-87 liquid detergent.

EXAMPLE VII A 100 ml. reaction flask is fitted with a mechanical stirrer, condenser, and thermometer, and 2.5 g. of hexahydropentamethylindane as produced in Example I and 2.5 g. of palladium on carbon catalyst containing 10% palladium are charged to the flask. The flask contents are brought to 234 C. and refluxed at that temperature for two hours until no further reaction is evident.

The catalyst is then filtered oif and the filtrate is analyzed. The product obtained is largely l,l,2,3,3-penta methylindane.

EXAMPLE VIII 1,l,2,3,3-pentamethylindane is treated With lithium in ammonia for thirty minutes at 33 C. The product is analyzed and found to contain 5,7a-dihydro-1,1,2,3,3- pentamethylindane. The dihydroindane so produced has an amber woody fragrance character suitable for incorporation into perfume compositions such as that set forth in Example III.

EXAMPLE IX An aliquot of the dihydroindane derivative produced 1n Example VIII is treated by dissolving lithium in ethylamine until the blue color disappears from the mass and 7 then adding the dihydro material with stirring and continuing the stirring under reflux for one hour.

The ethylamine is evaporated, water is added, and the aqueous mixture is extracted with hexane. The product is found to contain 3a,4-dihydro-1,1,2,3,3-pentamethylindane. This has an amber woody fragrance character suitable for incorporation into perfume compositions such as that set forth in Example III.

What is claimed is:

1. An indane derivative selected from the group consisting of 5,7a-dihydro-1,1,2,3,3-pentamethylindane; 3a,4- dihydro-1,1,2,3,3pentamethylindane; 4,5,6,7-tetrahydro- 1,1,2,3,3 -pentamethy1indane; and hexahydro-l,l,2,3,3- pentamethylindane.

2. A mixture of 4,5,6,7-tetrahydro-1,1,2,3,3-pentamethylindane and hexahydro-1,11,2,3,3-pentamethylindane obtained by the hydrogenation of 1,1,2,3,3-pentamethylindane.

3. An indane derivative as defined in claim 1, wherein said derivative is 5,7a-dihydro-1,1,2,3,3pentamethylindane.

4. An indane derivative as defined in claim 1, wherein said derivative is 3a,4-dihydro-1,l,2,3,3-pentamethylin dane.

5. An indane derivative as defined in claim 1, wherein said derivative is 4,5,6,7-tetrahydro-1,1,2,3,3pentamethylindane.

6. An indane derivative as defined in claim 1, wherein said derivative is hexahydro-l,1,2,3,3-pentamethylindane.

References Cited UNITED STATES PATENTS 3,636,176 1/1972 Hall 260-666 PY 2,249,987 7/ 1941 Stanley et a1 260-666 PY 3,183,249 5/1965 Wiese 2 60666 PY DELBERT E. GANTZ, Primary Examiner V. OKEEFE, Assistant Examiner US. Cl. X.R. 252522