Classifications

• • A—HUMAN NECESSITIES
  • A24—TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
  • A24B—MANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
  • A24B15/00—Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
  • A24B15/18—Treatment of tobacco products or tobacco substitutes
  • A24B15/28—Treatment of tobacco products or tobacco substitutes by chemical substances
  • A24B15/30—Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
  • C07C2/02—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons
  • C07C2/04—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation
  • C07C2/38—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of dienes or alkynes
  • C07C2/40—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms by addition between unsaturated hydrocarbons by oligomerisation of well-defined unsaturated hydrocarbons without ring formation of dienes or alkynes of conjugated dienes
  • C07C2/403—Catalytic processes

Definitions

• This invention has to do with a tobacco or tobacco-like product having improved smoking characteristics. More particularly, it relates to enhancing the flavor of tobacco containing products and to a process for making tobacco flavoring agents.
• tobacco means and includes, where the context permits, natural tobaccos such as burley, Turkish tobacco, Maryland tobacco, Virginia tobacco, and flue-cured tobacco; tobacco-like products such as reconstituted tobacco or homogenized tobacco; and tobacco substitutes intended to replace natural tobacco such as various vegetable leaves such as lettuce and cabbage leaves.
• tobacco materials can be improved in flavor and smoking characteristics by incorporating in, or adding to, such materials a small but effective amount of a polyisoprenoid hydrocarbon or a mixture of a plurality of such polyisoprenoid hydrocarbons.
• tobacco and tobacco-like materials are enhanced in flavor when admixed with a composition comprising certain polyisoprenoid hydrocarbons and certain polyisoprenoid esters or polyisoprenoid alcohols or mixtures of said esters and.
• Tobacco or tobacco-like products containing such a polyisoprenoid hydrocarbon, or mixtures of a polyisoprenoid hydrocarbon and a polyisoprenoid ester or a polyisoprenoid alcohol are less harsh, more mild and have a strong tobacco taste and character and this improved taste, character and flavor is noted although the tobacco is smoked through a filter.
• Still another aspect of this invention is the preparation of mixtures of the tobacco flavoring agents found useful in accordance with this invention by refining, without degrading, as by molecular distillation, crude mixtures of polyisoprenoid hydrocarbons and polyisoprenoid esters formed as a residue after removing the conventionally distillable components of the reaction products obtained by the controlled polymerization of isoprene.
• the polyisoprenoid hydrocarbons found effective as tobacco flavoring agents are represented by the formula H oH2-o--oH,- om H i: ('JH 1. where n is an integer of from about 4 to 15 inclusive and the dotted line means that, at the: position indicated, the bond can be either a single or a double bond, one double bond being present, and where x is an integer of 1 or 2 and y is an integer of 2 or 3, the value of x and y being determined by the position of the double bond.
• the data obtained from Nuclear Magnetic Resonance studies confirms the ptesence of vinylidene methylene groups as well as of tri-substituted double bonds.
• hydrocarbons formed may contain a terminal menthadiene group of the formula in place of the terminal hydrogen shown in the above formula. Accordingly the formula given as representative of the polyisoprenoid hydrocarbons contemplates and includes all of the foregoing variations.
• Such polyisoprenoid hydrocarbons include: 2,6,10,l4-tetramethyl-2,6, 10,14-hexadecatetraene; 2,6,10,14,18,22,26-heptamethyl- 2,6,10,14,l8,22,26-octa-cosaheptaene; 2,6,10,14,18,22,26,- 30,34-nona-methyl-2,6,10,14,18,22,26,30,34 hexatriacontanonaene; 2,6,10,14,18,22,26,30,3-4,38,42,46-dodecamethyl 2,6,l0,14,18,22,26,30,34,38,4-2,26 octatetradodeC- acne, and the double bond isomers thereof.
• a plurality of such hydrocarbons may be used, and preferably the molecularly distilled or purified mixture of hydrocarbons obtained from the controlled polymerization of isoprene is employed as the tobacco flavor
• polyisoprenoid hydrocarbons of this invention and mixtures of such hydrocarbons with polyisoprenoid esters or polyisoprenoid alcohols have been found to possess a combination of properties which make them particularly suitable as tobacco flavoring agents in that such compositions are effective at low concentrations and thus will not bleed into tobacco wrapping materials, are low in cost, are stable on prolonged storage, resemble natural constituents of tobacco, are not known to decompose on smoking to give materials which are physiologically harmful, and their flavor enhancement is deliverable through a filter.
• the use of the polyisoprenoid hydrocarbons of this invention and mixtures thereof as tobacco flavoring agents also permits greater flexibility in experimenting with new blends of tobacco.
• polyisoprenoid hydrocarbons of this inventon may also be admixed with other polyisoprenoid materials such as polyisoprenoid esters or alcohols or mixtures of such polyisoprenoid esters and alcohols, and such mixtures of polyisoprenoid hydrocarbon and other polyisoprenoid materials have been found to be particularly convenient compositions to be used as tobacco flavoring agents.
• n is an integer of from 4 to 15, inclusive
• R is an hydroxyl radical or a lower aliphatic carboxylic acid ester radical such as formate, acetate, propionate and the like
• the dotted line means that, at the positions indicated, the bond can be either a single or a double bond, one double bond being present, and where x is an integer of 1 or 2 and y is an integer of 2, or 3, the value of x and y being determined by the position of the double bond.
• the data obtained from Nuclear Magnetic Resonance studies confirms the presence of vinylidene methylene groups as well as of tri-substituted double bonds.
• esters or alcohols formed may contain a terminal menthadiene group of the formula in place of the terminal hydrogen shown in the above formula. Accordingly the formula given as representative of the polyisoprenoid esters or alcohols contemplates and includes all of the foregoing variations.
• Such polyisoprenoid alcohols include: 2,6,10,14-tetramethyl- 2,6, 10, l4-hexadecatetraene-1 6-01; 2,6, 10,14,18,22,26-heptamethyl-2,6,l0,14,18,22,26-octacosaheptaene-28-01; 2,6, 10,14,18,22,26,30,34-nonomethyl 2,6,10,14,18,22,26,30, 34-hexatriacontanonaen 36-01; 2,6,l0,14,18,22,26,30,34, 38,42,46-octatetracontadodecaen-48-ol; and the double bond isomers thereof.
• the polyisoprenoid esters include the lower alkyl esters of the aforesaid alcohols. It should be understood that the useful polyisoprenoid alcohols represented by the above formula may include additional hydroxy groups in the chain or may have tertiary hydroxy groups rather than terminal hydroxy groups and such materials would be considered equivalent for purposes of this invention.
• the mixture of polyisoprenoid hydrocarbon and other polyisoprenoid material may contain a broad range of amounts by weight of polyisoprenoid hydro-- carbon to other polyisoprenoid material, it is convenient that the polyisoprenoid hydrocarbon be present in a minor amount (less than 50%) by weight and the other polyisoprenoid materials in the mixture be present in a major amount (50% or more) by weight since such compositions may be directly prepared by the controlled polymerization of isoprene in a lower aliphatic carboxylic acid. More particularly, the polyisoprenoid hydrocarbon may range from about to 40 percent by weight of the total polyisoprenoid mixture and the other polyisoprenoid material may range from about 85 to 60 percent by Weight of the total mixture.
• the tobacco flavoring agent composition of this invention may be incorporated in, or added to, tobacco products by any of the usual techniques including mechanical mixing, spraying, impregnation, coating and I other methods which will readily occur to those skilled in the art.
• the amount of the tobacco flavoring agent composition used will depend upon a number of factors including: the particular flavor or smoking character desired, the particular tobaccos used, and the specific flavor agent composition employed.
• the flavor agent mixture of this invention is admixed with tobacco or tobacco-like materials in amounts of from about 0.25 to 6.0 percent by weight based on the weight of the tobacco materials. At proportions below about 0.25 percent little improvement is detected and at proportions much above about 6.0 percent nontobacco or objectionable flavors or aromas may be produced.
• the tobacco enhancing compositions of this invention may also be combined with other flavor or aroma enhancing materials to obtain a more esthetically pleasing combination of qualities. These can be formulated as desired to obtain the particular nuances required.
• Other smoke enhancing ingredients with which the compositions of this invention may be combined include: essential oils, balsams, fruit flavors such as peach, walnut and cherry, coriander, coumarin, lactic acid and phenylacetic acid. Minty, spicy, nutty, fruity, and many other nuances can be added to the compositions of this invention.
• a mixture of polyisoprenoid hydrocarbons of suitable chain length may be prepared by the controlled polymerization of isoprene.
• ionic polymerizations have been found to be more capable of being controlled, and, therefore, are to be preferred in the practice of this invention.
• a useful mixture of such polyisoprenoid hydrocarbons and polyisoprenoid esters may be obtained directly by the controlled polymerization of isoprene in a lower aliphatic carboxylic acid.
• reaction mixture containing the desired polyisoprenoid materials of suitable chain length (C to C are refined and separated from the non-distillable portions in such a manner that the mixture is purified under low thermal hazard conditions so that the material is not decomposed or degraded.
• Molecular distillation procedures have been found to be particularly effective in separating the desired polyisoprenoid materials from the undistillable objectionable portions of the reaction product components without degradation of the desired polyisoprenoid materials.
• the spinning disc type of molecular still has been especially effective since it permits purification with the least thermal degradation, although, the wiping or brush type molecular still may be used.
• the controlled polymerization is of the ionic type, and is preferably carried out by reacting isoprene in a lower aliphatic carboxylic acid and in the presence of a strong acid catalyst, preferably having a pH of 3 or less, under controlled temperatures and for a period suflicient to obtain the desired chain length.
• a strong acid catalyst preferably having a pH of 3 or less
• Any lower aliphatic carboxylic acid may be used, although lower alkyl monocarboxylic acids such as acetic acid, propionic acid and the like are preferred.
• the strong acid catalyst used may be a mineral acid such as sulfuric acid and phosphoric acid, or acidic resins such as sulfonated polystyrene resins like Amberlyst 15 made and sold by Rohm & Haas Company, and other strong acid equivalents.
• the temperature and duration of the reaction will depend on a variety of factors including the economics of reaction time and conversions desired, and the specific organic acid and catalyst employed. Generally, the reaction temperature may vary from about C. to 70 C. and temperatures of from about 25 C. to 35 C. are preferred since at lower temperatures the reaction time is slowed, while at temperatures much above 70 C. the reaction may proceed too quickly, higher polymers of isoprene may be formed, and a closed system and super atmospheric pressure is required to prevent loss of the volatile isoprene.
• the time of the reaction may vary from about 5 to 200 hours, and preferably the reaction period is from about 50 to 170 hours.
• the acid catalyst is neutralized by the addition of a basic material or removed from the reaction mixture, and the unreacted materials and the reaction products of chain length below about C may be separated by any conventional method.
• such products are separated by distillation.
• the residue from this separation containing products of about C and higher chain lengths is further refined by molecular distillation, and the distillate from this molecular distillation contains a tobacco flavor agent composition comprising the polyisoprenoid hydrocarbons and polyisoprenoid esters of this invention and the composition obtained may be used as such without further treatment.
• the polyisoprenoid hydrocarbons are the preferred flavoring agents
• the polyisoprenoid esters formed in the reaction may be converted, if desired, to the corresponding polyisoprenoid hydrocarbons by pyrolysis or any of the conventional processes.
• the said composition of polyisoprenoid hydrocarbons and polyisoprenoid esters may be saponified by reaction with a strong alkali-material to yield a mixture of polyisoprenoid hydrocarbons and polyisoprenoid alcohols, which may also contain some polyisoprenoid esters depending upon the degree of hydrolysis obtained.
• the saponified mixture after purification by molecular distillation is also effective as a tobacco enhancing agent.
• the catalyst was then neutralized by adding 50 gm. of anhydrous sodium acetate to the mixture, and the mixture was stirred until the salt was dissolved.
• the reflux condenser was replaced with a distillation head and the reaction mixture heated to 50 C. A fraction weighing 703 gm. was obtained. This fraction was essentially pure isoprene.
• the pressure was held at 3 mm. Hg and the temperature of the reaction mixture slowly raised to 200 C.
• the distilled fraction was condensed and collected. It Weighed 942 gm. The residue weighed 256 gm.
• Example 2 To 5 kg. of the residue of Example 1 was added 8 liters of 20% potassium hydroxide in methanol. The reaction mass was then neutralized with hydrochloric acid, washed with water and extracted with petroleum ether. The ether extract was dried and flash evaporated leaving 4,176 grams of a crude mixture. The crude mixture was then molecularly distilled on a spinning disc molecular distillation unit and yielded a composition composed of about 30% by weight of C to C polyisoprenoid hydrocarbons and 70% by weight of C to C polyisoprenoid alcohols.
• Example 2 The 4,176 grams of saponified product of Example 2 was diluted with 6 liters of n-hexane, and 20 pounds of activated silica gel was slowly added with stirring. The silica gel was filtered and washed with 10 liters of hexane. The wash and filtrate were combined and flash evaporated, yielding 1,817 grams of hydrocarbon material.
• the silica gel was then washed with 12 liters of methanol.
• the wash liquid was flash evaporated leaving 1,396 grams of crude alcohols. This material was distilled on a spinning disc molecular still. Twelve fractions weighing 916 grams were obtained;
• the reflux condenser was replaced with a distillation head and condenser and the reaction mixture heated to 50 C.
• the residue was distilled on a spinning disc molecular distillation unit.
• the resulting product comprised a mixture of C to C polyisoprenoid hydrocarbons and a mixture of C to C polyisoprenoid propionates, in which the ester proportion of the mixture represented about 70 percent by weight.
• Example 2 The resulting product may then be saponified as in Example 2 and separated into hydrocarbon and alcohol fractions in accordance with the procedure set forth in Example 3.
• EXAMPLE 5 A series of tobacco blends were prepared by spraying a solution of each of the flavoring agents shown in the following tabulation onto a tobacco blend consisting of by weight of Type 12 Virginia tobacco and 45% by weight of Burley tobacco. The solution comprised one percent of each of said flavoring agents based on the weight of the tobacco blend and equal parts by volume of hexane and special denatured number 4 ethyl alcohol. Each of the sprayed tobacco blends was air dried, made into cigarettes and allowed to age over night. The cigarettes were then smoked and evaluated by a panel of experts and the results indicated in the tabulation were noted.
• Flavoring agent employed Evaluation comment 1 comprising a mixture of 020 to C polyisocant ofi taste, less harsh.
• prenoid hydrocarbons and a mixture of C20 to C15 polyisoprenoid acetates.
• Hydrocarbon fraction 7 of Example 3 Strong tobacco flavor. Milder flavor. Smoother than flavoring agent 2 of this tabulation.
• Example (14) Alcohol fraction 5 of Example 3 (12) Strong flowery, chemical ofi taste. (11;) Composite 0f 12 alcohol fractions of Example (13) Some 011 taste. Not suitable at w (14)
• the moleeularly distilled product of Example (14) 2 comprising a mixture of 010-0 polyisoprenoid hydrocarbons alcohols.
• Ci -C polyisoprenoid Agents Nos. 2 and 3 of this tabulation.
• the pressure was held at 3 mm. Hg and the temperature of the liquid slowly raised from 50 C. to 200 C. A fraction weighing 277 grams was collected. As residue, 192 grams were obtained.
• the distilled fraction was washed once with 600 ml. of water and then once with 600 m1. of 3% aqueous so- EXAMPLE 6 r 0 gm. of anhydrous sodium acetate was then added to the mixture and stirred until dissolved.
• the reflux condenser was replaced with a distillation head and condenser and the reaction mixture heated to 50 C. A fraction of pure isoprene weighing 592 gm. was obtained.
• the pressure was reduced to 100 mm. Hg and the temperature of the reaction mixture held at 50 C. A fraction weighing 672 gm. and consisting of 325 gm. (48.4%) of acetic acid and 347 gm. (51.6%) of isoprene was obtained. The reaction mixture was cooled and filtered under slight vacuum to remove the ion-exchange resin. The filtrate was distilled at a pressure of 3 mm. Hg maintaining the reaction mixture at 50 C. A fraction weighing 2363 gm. and consisting of 1,914 gm. (81%) of acetic acid and 449 gm. (19%) of prenylacetate was obtained. The pressure was held at 3mm. and the temperature of the liquid slowly raised from 50 C. to 200 C. A fraction weighing 569 gm. was obtained. A residue of 55 gm. was obtained.
• the residue of 55 gm. may then be distilled on a spinning disc molecular still.
• the resulting distilled product comprises a mixture of C to C polyisoprenoid hydrocarbons and a mixture of C to C polyisoproprenoid acetates, in which the ester portion of the mixture represents about 70 percent by weight.
• the distilled mixture is blended with tobacco at one percent by weight concentration and enhances the flavor of the blend when smoked.
• EXAMPLE 7 4 kg. of the residue obtained in Example 1 was distilled on a spinning disc molecular distillation unit as described in Example 1, yielding 3.2 kg. of distilled product comprising a mixture of C to C polyisoprenoid hydrocarbons and a mixture of 0 to C polyisoprenoid acetates, in which the ester portion of the mixture represented about 70 percent by weight.
• This material was passed through a steel tube packed with porcelain saddles at 400 C. in a nitrogen atmosphere, yielding about 1,400 gm. of a product consisting substantially of polyisoprenoid hydrocarbons having the same chain length as the hydrocarbons of Example 3.
• the crude pyrolysate mixture was washed with aqueous sodium bicarbonate solution to remove the acetic acid formed in the pyrolysis, dried, and distilled on a spinning disc as in Example 3. There were obtained 11 fractions in a temperature range of 85 C. to 185 C. (rotor temperature) at approximately .03 to .02 mm. Hg pressure. Of these fractions, the first three were discarded. The remainder of about 1100 gm. were evaluated and were found to have substantially the same smoking properties as the product of Example 3.
• a composition suitable for flavoring tobacco products consisting essentially of a molecularly distilled purified mixture of (i) a polyisoprenoid hydrocarbon represented by the formula wherein n is an integer of from about 4 to 15, and wherein each dotted line is a bond selected from the group consisting of a single bond and a double bond, a double bond being present, and wherein x is an integer of from 1 to 2 and y is an integer of from 2 to 3, the value of x and y being determined by the position of said double bond, and (ii) a polyisoprenoid compound selected from the group consisting of (A) polyisoprenoid esters of th formula i: 6 wherein n is an integer of from 4 to 15 and R is a lower alkyl radical, and wherein each dotted line is a bond selected from the group consisting of a single bond and a double bond, a double bond being present, and wherein x is an integer of from 1 to 2 and ;y is an integer of from 2 to
• composition as defined in claim 1, wherein said polyisoprenoid hydrocarbon is in. an amount of from about 15 to 40 percent by weight of said total composition.
• composition as defined in claim 1, wherein said polyisoprenoid compound is a polyisoprenoid ester.
• composition as defined in claim 1, wherein said polyisoprenoid compound is a polyisoprenoid alcohol.
• a process for preparing a composition comprising a purified mixture of (i) a polyisoprenoid hydrocarbon of the formula wherein n is an integer of from about 4 to 15 inclusive, and wherein each dotted line is a bond selected from the group consisting of a single bond and a double bond, a double bond being present, and wherein x is an integer of from 1 to 2 and y is an integer of from 2 to 3, the value of x and y being determined by the position of said double bond, and (ii) a polyisoprenoid ester represented by the formula 0 H -CH2( 7--CHr-CH2 O(
• a process for preparing a composition comprising a 1 l purified mixture of (i) a polyisoprenoid hydrocarbon of the formula H[-OHz "CHx-CH2]H on, n wherein n is an integer of from about 4 to 15 inclusive, and wherein each dotted line is a bond selected from the group consisting of a single bond aniia double bond, a double bond being present, and wherein x is an integer of from 1 to 2 and y is an integer of from 2 to 3, the value of x and y being determined by the position of said double bond, and (ii) a polyisoprenoid alcohol represented by the formula H[CH2( 3--CH;CH2]OH on, n
• n is an integer of from about 4 to 15 inclusive and wherein each dotted line is a bond selected from the group consisting of a single bond and a double bond, a double bond being present, and wherein x is an integer of from 1 to 2 and y is an integer of from 2 to 3, the value of x and y being determined by the position of said double bond, which comprises polymerizing isoprene at controlled conditions at a temperature of from about 15 C. to 70 C.

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Citations (2)

• 1965
  • 1965-02-16 US US433174A patent/US3542677A/en not_active Expired - Lifetime
  • 1965-11-25 GB GB50219/65A patent/GB1087774A/en not_active Expired
  • 1965-12-07 IT IT27028/65A patent/IT943016B/it active
  • 1965-12-15 FR FR42475A patent/FR1459675A/fr not_active Expired
  • 1965-12-16 DE DE19651517291 patent/DE1517291A1/de active Pending
  • 1965-12-21 NL NL6516640A patent/NL6516640A/xx unknown
  • 1965-12-21 BE BE674116D patent/BE674116A/xx unknown
  • 1965-12-21 CH CH1762765A patent/CH477829A/de not_active IP Right Cessation

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