US3217716A - Tobacco composition - Google Patents

Tobacco composition Download PDF

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Publication number
US3217716A
US3217716A US323599A US32359963A US3217716A US 3217716 A US3217716 A US 3217716A US 323599 A US323599 A US 323599A US 32359963 A US32359963 A US 32359963A US 3217716 A US3217716 A US 3217716A
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United States
Prior art keywords
tobacco
added
percent
tetramethyl
domestic
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Expired - Lifetime
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US323599A
Inventor
Donald L Roberts
Joseph N Schumacher
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
RJ Reynolds Tobacco Co
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RJ Reynolds Tobacco Co
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Publication date
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Priority to US323599A priority Critical patent/US3217716A/en
Priority to GB44253/64A priority patent/GB1016090A/en
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Publication of US3217716A publication Critical patent/US3217716A/en
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Classifications

    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/30Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
    • A24B15/36Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a heterocyclic ring
    • A24B15/40Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a heterocyclic ring having only oxygen or sulfur as hetero atoms
    • A24B15/403Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances containing a heterocyclic ring having only oxygen or sulfur as hetero atoms having only oxygen as hetero atoms
    • AHUMAN NECESSITIES
    • A24TOBACCO; CIGARS; CIGARETTES; SIMULATED SMOKING DEVICES; SMOKERS' REQUISITES
    • A24BMANUFACTURE OR PREPARATION OF TOBACCO FOR SMOKING OR CHEWING; TOBACCO; SNUFF
    • A24B15/00Chemical features or treatment of tobacco; Tobacco substitutes, e.g. in liquid form
    • A24B15/18Treatment of tobacco products or tobacco substitutes
    • A24B15/28Treatment of tobacco products or tobacco substitutes by chemical substances
    • A24B15/30Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances
    • A24B15/301Treatment of tobacco products or tobacco substitutes by chemical substances by organic substances by aromatic compounds

Definitions

  • An additional object of this invention is to provide a tobacco which has been treated in such manner as to impart an aroma which is pleasing to the smoker and is described by some as a camphoraceous aroma.
  • a domestic tobacco is provided to which has been added a small amount of hexahydro-2,5,5,8a-tetramethyl-7- chromanone.
  • the above chemical herein referred to as compound I, may be represented by the following formula:
  • the chemical compound I indicated above can be synthesized by oxidizing dihydro-a-ionone to form 5- oxodihydro-a-ionone and reducing the so-formed dihydro-w-ionone to 5-OXOdlhYdIO-oc-l0ll0l which, by treating with acid, undergoes rearrangement to form compound I.
  • Compound I is a solid having a melting point of 4041 C. and is further characterized as follows:
  • the designated compound I is usually added to a domestic tobacco in amounts to provide a tobacco in which is dispersed about 0.001 to about 1.0 percent by weight of the additive.
  • the amount of additive is between about 0.005 and about 0.03 percent by weight in order to form a domestic tobacco having a desired flavor and aroma.
  • the preferred percentages may be somewhat less, however, if other flavorants imparting a desired aroma are also employed.
  • the additive may be applied in any suitable manner and preferably in the form of a liquid solution or suspension by spraying, dipping or otherwise.
  • the additive may be incorporated at any step in the treatment of the tobacco but is preferably added after aging, curing and shredding and before the tobacco is formed into cigarettes.
  • the tobacco treated may have the additive in excess of the amounts above indicated so that when blended with other tobaccos the final product will have the percentage within the indicated range.
  • the manner in which the additive is applied to the tobacco is not particularly important since, as indicated, it may be done in the form of spraying or dipping, utilizing suitable suspensions or solutions of the additive.
  • water or volatile organic solvents such as alcohol, ether, acetone, volatile hydrocarbons and the like, may be used as the carrying medium for the additive while it is being applied to the tobacco.
  • other flavor and aroma producing additives such as those disclosed in Jones United States Patent No. 2,766,145 and Schumacher United States Patent No. 2,978,365, may be incorporated into the tobacco with the additives of this invention.
  • the additive of the invention being appreciably volatile, can be incorporated with materials such as filter tip materials, seam paste, packaging materials and the like which are used along with tobacco to form a product adapted for smoking.
  • the compound may be added to certain tobacco substitutes of natural or synthetic origin and by the term tobacco as used throughout this specification is meant any composition intended for human consumption by smoking or otherwise, Whether composed of tobacco plant parts or substitute materials or both.
  • a domestic smoking tobacco having added thereto between about 0.001 and 1.0 percent by weight of hexahydro-2,5,5,8a-tetramethyl-7-chromanone.
  • a tobacco product having added thereto a small amount of heXahydro-2,5,5,8a-tetramethyl-7-chromanone sufficient to improve the flavor of the tobacco product.
  • a product adapted for smoking having added thereto a small amount of heXahydr0-2,5,5,8a-tetramethyl-7- chromanone suflicient to improve the flavor of the smoking product.
  • a tobacco product having added thereto between about 0.001 and about 1.0 percent by weight of hexahydro-2,5,5,8a-tetramethyl-7-chroman0ne.
  • a product adapted for smoking having added thereto between about 0.001 and about 1.0 percent by weight of heXahydro-2,5,5,8a-tetramethyl-7-chr0manone.
  • a domestic smoking tobacco having added thereto between about 0.005 and about 0.03 percent by weight of hexahydro-Z,5,5,8a-tetramethyl-7-chromanone.

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  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Manufacture Of Tobacco Products (AREA)

Description

United States Patent 3,217,716 TOBACCO COMPOSITION Donald L. Roberts and Joseph N. Schumacher, Winston- Salem, N.C., assignors to R. J. Reynolds Tobacco Company, Winston-Salem, N.C., a corporation of New Jersey No Drawing. Filed Nov. 14, 1963, Ser. No. 323,599 9 Claims. (Cl. 13117) This invention relates to tobacco and has for an object the provision of a tobacco composition having an improved aroma and flavor.
It is well known in the tobacco art that the domestic tobaccos which are exemplified by burley, Maryland, fluecured, bright leaf or Virginia tobaccos .are low in flavor as compared with so-called oriental or aromatic tobaccos which are imported from Turkey, Greece, Bulgaria, Yugoslavia, Rhodesia and Russia. Accordingly, it has been common practice in the tobacco industry to prepare blends of domestic and oriental tobaccos in order to provide cigarettes which have desired flavor and aroma characteristics. Accordingly, it is a further object of this invention to provide a domestic tobacco which has an enhanced flavor and aroma.
An additional object of this invention is to provide a tobacco which has been treated in such manner as to impart an aroma which is pleasing to the smoker and is described by some as a camphoraceous aroma.
In accordance with one embodiment of this invention, a domestic tobacco is provided to which has been added a small amount of hexahydro-2,5,5,8a-tetramethyl-7- chromanone. The above chemical, herein referred to as compound I, may be represented by the following formula:
The chemical compound I indicated above can be synthesized by oxidizing dihydro-a-ionone to form 5- oxodihydro-a-ionone and reducing the so-formed dihydro-w-ionone to 5-OXOdlhYdIO-oc-l0ll0l which, by treating with acid, undergoes rearrangement to form compound I.
A detailed description of the synthesis of compound I is as follows:
A. Dihydro-a-ionone (85 grams) made by hydrogenation of a-ionone, as in known, was oxidized using t-butyl chromate in benzene solution for a period of four lays at room temperature. Chromatography of the products from the oxidation gave 20 grams of dihydro-a-ionone, grams of 5-oxodihydro-wionone, and numerous side products.
B. 5-Oxodihydro-a-ionone (8.5 grams) was dissolved in 50 percent aqueous methanol (100 milliliters) and 0.4 gram of sodium borohydride was added. After 3 hours at room temperature, 5 percent sodium hydroxide was added and the solution was extracted with ether. After drying and evaporating the solvent, the residue was chromatographed; 8 grams of 5-oxodihydro-u-ionol was obtained. The product was identified by its infrared and nuclear magnetic resonance spectra.
C. The 5-oxodihydro-a-ionol from above was dissolved in benzene and 0.2 gram of p-toluenesulfonic acid was added. The solution was refluxed for one hour; then it was extracted with sodium carbonate solution and the organic layer was chromatographed on silicic acid. The products, eluted from the column with ether-pentane mixtures, were identified as compound I, S-oxodihydrowionol and side products. The yield of compound I was about 40% based on 5-oxodihydro-a-iono1 consumed.
Compound I is a solid having a melting point of 4041 C. and is further characterized as follows:
Infrared spectrum: 1708, 1280', 1264, 1095, 1050 and 970 cm.-
NMR spectrum: 726.2241), 7.47(2), 7.70(2), 8.78 (3), 8.87(3 doublet), 893(3), and 920(3).
Analysis.Calcd. for C H O C, 74.24; H, 10.54; Mol wt. 210. Found: C, 74.01; H, 10.53; Mass 210.
In accordance with this invention, the designated compound I is usually added to a domestic tobacco in amounts to provide a tobacco in which is dispersed about 0.001 to about 1.0 percent by weight of the additive. Preferably the amount of additive is between about 0.005 and about 0.03 percent by weight in order to form a domestic tobacco having a desired flavor and aroma. The preferred percentages may be somewhat less, however, if other flavorants imparting a desired aroma are also employed. The additive may be applied in any suitable manner and preferably in the form of a liquid solution or suspension by spraying, dipping or otherwise. The additive may be incorporated at any step in the treatment of the tobacco but is preferably added after aging, curing and shredding and before the tobacco is formed into cigarettes. Likewise, it will be apparent that only a portion of the domestic tobacco need be treated and the thus treated tobacco may be blended with other tobaccos before the cigarettes are formed. In such cases the tobacco treated may have the additive in excess of the amounts above indicated so that when blended with other tobaccos the final product will have the percentage within the indicated range.
In accordance with one specific example of this in vention, an aged, cured and shredded burley tobacco is sprayed with a one percent ethyl alcohol solution of the above indicated compound in an amount to provide a tobacco composition containing 0.01 percent by weight of the additive on a dry basis. Thereafter the alcohol is removed by evaporation and the tobacco is manufactured into cigarettes by the usual techniques. The cigarette, when treated as indicated, has a desired and pleasing aroma which is described by some as camphoraceous and which is detectable to some extent when the cigarette is in its package but which is particularly detectable and pleasing in the main and side smoke streams when the cigarette is smoked.
It will be particularly apparent that the manner in which the additive is applied to the tobacco is not particularly important since, as indicated, it may be done in the form of spraying or dipping, utilizing suitable suspensions or solutions of the additive. Thus water or volatile organic solvents, such as alcohol, ether, acetone, volatile hydrocarbons and the like, may be used as the carrying medium for the additive while it is being applied to the tobacco. Also, other flavor and aroma producing additives, such as those disclosed in Jones United States Patent No. 2,766,145 and Schumacher United States Patent No. 2,978,365, may be incorporated into the tobacco with the additives of this invention.
While this invention is particularly useful in the manufacture of cigarette tobacco, it is also suitable for use in connection with the manufacture of pipe tobacco, cigars and other tobacco products formed from sheeted tobacco dust or fines which are well known to the art. Likewise, the additive of the invention, being appreciably volatile, can be incorporated with materials such as filter tip materials, seam paste, packaging materials and the like which are used along with tobacco to form a product adapted for smoking. Furthermore, the compound may be added to certain tobacco substitutes of natural or synthetic origin and by the term tobacco as used throughout this specification is meant any composition intended for human consumption by smoking or otherwise, Whether composed of tobacco plant parts or substitute materials or both.
Those modifications and equivalents which fall within the spirit of the invention and the scope of the appended claims are to be considered part of the invention.
We claim:
1. A domestic tobacco having added thereto a small amount of hexahydro-Z,5,5-8a-tetramethyl-7-chnomanone suificient to alter the flavor of the tobacco.
2. A domestic smoking tobacco having added thereto between about 0.001 and 1.0 percent by weight of hexahydro-2,5,5,8a-tetramethyl-7-chromanone.
3. A tobacco product having added thereto a small amount of heXahydro-2,5,5,8a-tetramethyl-7-chromanone sufficient to improve the flavor of the tobacco product.
4. A product adapted for smoking having added thereto a small amount of heXahydr0-2,5,5,8a-tetramethyl-7- chromanone suflicient to improve the flavor of the smoking product.
5. A tobacco product having added thereto between about 0.001 and about 1.0 percent by weight of hexahydro-2,5,5,8a-tetramethyl-7-chroman0ne.
6. A tobacco product having added thereto between about 0.005 and about 0.03 percent by Weight of heXahydro-2,5,5,8a-tetramethyl-7-chromanone.
7. A product adapted for smoking having added thereto between about 0.001 and about 1.0 percent by weight of heXahydro-2,5,5,8a-tetramethyl-7-chr0manone.
8. A product adapted for smoking having added thereto between about 0.005 and about 0.03 percent by weight of heXahydro-2,5,5,8a-tetramethyl-7-chromanone.
9. A domestic smoking tobacco having added thereto between about 0.005 and about 0.03 percent by weight of hexahydro-Z,5,5,8a-tetramethyl-7-chromanone.
References Cited by the Examiner UNITED STATES PATENTS 3,126,012 3/1964 Jarboe et a1. 131l7 ABRAHAM G. STONE, Primary Examiner.
F. RAY CHAPPELL, Examiner.

Claims (1)

1. A DOMESTIC TOBACCO HAVIN ADDED THERETO A SMALL AMOUNT OF HEXAHYDRO-2,5,5-8A-TETRAMETHYL-7-CHROMANONE SUFFICIENT TO ALTER THE FLAVOR OF THE TOBACCO.
US323599A 1963-11-14 1963-11-14 Tobacco composition Expired - Lifetime US3217716A (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
US323599A US3217716A (en) 1963-11-14 1963-11-14 Tobacco composition
GB44253/64A GB1016090A (en) 1963-11-14 1964-10-29 An improved tobacco, products comprising the improved tobacco and process for improving tobacco

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3389706A (en) * 1965-11-08 1968-06-25 Reynolds Tobacco Co R Tobacco product
US3563248A (en) * 1969-05-16 1971-02-16 Brown & Williamson Tobacco Tobacco product

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3126012A (en) * 1964-03-24 Smqeong tobacco additives in the form

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3126012A (en) * 1964-03-24 Smqeong tobacco additives in the form

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3389706A (en) * 1965-11-08 1968-06-25 Reynolds Tobacco Co R Tobacco product
US3563248A (en) * 1969-05-16 1971-02-16 Brown & Williamson Tobacco Tobacco product

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Publication number Publication date
GB1016090A (en) 1966-01-05

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