EP1625106A4 - Novel fragrance derivatives - Google Patents

Novel fragrance derivatives

Info

Publication number
EP1625106A4
EP1625106A4 EP04760941A EP04760941A EP1625106A4 EP 1625106 A4 EP1625106 A4 EP 1625106A4 EP 04760941 A EP04760941 A EP 04760941A EP 04760941 A EP04760941 A EP 04760941A EP 1625106 A4 EP1625106 A4 EP 1625106A4
Authority
EP
European Patent Office
Prior art keywords
novel fragrance
fragrance derivatives
derivatives
novel
fragrance
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP04760941A
Other languages
German (de)
French (fr)
Other versions
EP1625106A2 (en
Inventor
Luca Turin
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.)
Flexitral Inc
Original Assignee
Flexitral Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Flexitral Inc filed Critical Flexitral Inc
Publication of EP1625106A2 publication Critical patent/EP1625106A2/en
Publication of EP1625106A4 publication Critical patent/EP1625106A4/en
Withdrawn legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D331/00—Heterocyclic compounds containing rings of less than five members, having one sulfur atom as the only ring hetero atom
    • C07D331/02—Three-membered rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D301/00—Preparation of oxiranes
    • C07D301/02—Synthesis of the oxirane ring
    • C07D301/03—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds
    • C07D301/14—Synthesis of the oxirane ring by oxidation of unsaturated compounds, or of mixtures of unsaturated and saturated compounds with organic peracids, or salts, anhydrides or esters thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02—Compounds containing oxirane rings
    • C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/14—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by free hydroxyl radicals
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0069—Heterocyclic compounds
    • C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
    • C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/50—Perfumes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Fats And Perfumes (AREA)
  • Epoxy Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Cosmetics (AREA)
  • Detergent Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
EP04760941A 2003-05-08 2004-05-07 Novel fragrance derivatives Withdrawn EP1625106A4 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US46866603P 2003-05-08 2003-05-08
PCT/US2004/014399 WO2004101472A2 (en) 2003-05-08 2004-05-07 Novel fragrance derivatives

Publications (2)

Publication Number Publication Date
EP1625106A2 EP1625106A2 (en) 2006-02-15
EP1625106A4 true EP1625106A4 (en) 2010-09-08

Family

ID=33452222

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04760941A Withdrawn EP1625106A4 (en) 2003-05-08 2004-05-07 Novel fragrance derivatives

Country Status (9)

Country Link
EP (1) EP1625106A4 (en)
JP (1) JP2007516956A (en)
KR (1) KR20060032136A (en)
CN (1) CN1925826A (en)
AU (1) AU2004238835A1 (en)
CA (1) CA2524897A1 (en)
GB (1) GB2419593B (en)
WO (1) WO2004101472A2 (en)
ZA (1) ZA200508991B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2005319103A1 (en) * 2004-12-22 2006-06-29 Flexitral Inc. Improved citral and citronellal derivatives
GB2423767B (en) * 2005-03-02 2007-07-18 Flexitral Inc Macrocyclic Thiiranes

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3166575A (en) * 1961-03-15 1965-01-19 Givaudan Corp 2(2-methyl-1-propene)-yl-4-methyl-tetrahydro-pyrans and 2(2-methyl-2-propene)-yl-4-methyl-tetrahydro-pyrans
US4429139A (en) * 1981-11-04 1984-01-31 Firmenich Sa Process for the preparation of rose oxide
US4478865A (en) * 1980-12-23 1984-10-23 Firmenich Sa Utilization of sulfur containing terpenes as flavoring ingredients

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2902495A (en) * 1956-04-09 1959-09-01 Glidden Co Treatment of certain derivatives of 2,6-dimethyl-octane and intermediates
US3927083A (en) * 1972-06-15 1975-12-16 Int Flavors & Fragrances Inc Bicyclic compounds and processes for making and using same
DE2617816A1 (en) * 1976-04-23 1977-11-10 Henkel & Cie Gmbh Perfume compsns. contg. epoxynitriles - are prepd. from ketones and chloro-acetonitrile and pref. contg. methyl gps. or alicyclic rings
US4162258A (en) * 1977-04-06 1979-07-24 The Lion Dentifrice Co., Ltd. Novel compounds spiro[5-isopropylbicyclo[3.1.0]hexane-2,2'-oxiranes], process for the production of the novel compounds, and process for the production of sabinene hydrates therefrom
JPS5466663A (en) * 1977-11-01 1979-05-29 Lion Dentifrice Co Ltd Method of manufacturing spiro*55isopropyl bicyclo*3*1*0*hexanee2*22oxilane*
IL63433A (en) * 1980-08-06 1986-04-29 Univ Leland Stanford Junior Method of asymmetrical epoxidation
JPS5735508A (en) * 1980-08-12 1982-02-26 Nippon Petrochem Co Ltd Perfumery composition containing glycidic acid ester
US4620945A (en) * 1983-08-01 1986-11-04 International Flavors & Fragrances Inc. Mixtures of one or more t-mercapto terpene isomers and α-terpineol, β-phenylethyl alcohol, 3-methyl-1-phenyl-pentanol-5 and/or butanoyl cyclohexane derivatives, organoleptic uses thereof and process for preparing same
DE3406999A1 (en) * 1984-02-27 1985-09-05 Hoffmann, Hans Martin Rudolf, Prof.PhD, DSc., 3004 Isernhagen Oxygenated tetramethyllimonene derivatives
JPS60190774A (en) * 1984-03-09 1985-09-28 Sagami Chem Res Center Produciton of epoxyalcohol
JPH06726B2 (en) * 1985-07-19 1994-01-05 株式会社クラレ Nitrogen-containing terpene alcohols and antiallergic agents containing the same
JPH04120071A (en) * 1990-09-10 1992-04-21 Dainippon Ink & Chem Inc Production of oxy compound
JP3434526B2 (en) * 1992-12-01 2003-08-11 三井化学株式会社 Method for producing epoxy-containing compound, α-hydroxycarbonyl compound or alkylsilyl or arylsilyl derivative of α-hydroxycarbonyl compound
ES2160044B1 (en) * 1999-03-16 2002-06-16 Univ Valencia Politecnica OXIDATION OF * -PINENE.
DE10055092A1 (en) * 2000-11-07 2002-05-08 Haarmann & Reimer Gmbh Preparing linalool oxide, useful as flavoring and perfume, by enzymatic oxidation of linalool, provides yields over 90 %
EP1601752B1 (en) * 2003-03-13 2010-01-13 Flexitral, Inc. Macrocyclic musks

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3166575A (en) * 1961-03-15 1965-01-19 Givaudan Corp 2(2-methyl-1-propene)-yl-4-methyl-tetrahydro-pyrans and 2(2-methyl-2-propene)-yl-4-methyl-tetrahydro-pyrans
US4478865A (en) * 1980-12-23 1984-10-23 Firmenich Sa Utilization of sulfur containing terpenes as flavoring ingredients
US4429139A (en) * 1981-11-04 1984-01-31 Firmenich Sa Process for the preparation of rose oxide

Non-Patent Citations (6)

* Cited by examiner, † Cited by third party
Title
A. TOMISEK: "the synthesis of ethylene oxide-1,2-c14", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY., vol. 73, 1951, USAMERICAN CHEMICAL SOCIETY, WASHINGTON, DC., pages 4685 - 4686, XP002593408, ISSN: 0002-7863 *
H. LEININGER ET AL.: "7-thiatetracyclo[4.1.0.02,4.03,5]heptan(benzvalensulfid)", BERICHTE DER DEUTSCHEN CHEMISCHEN GESELLSCHAFT., vol. 115, no. 10, 1982, DEVERLAG CHEMIE. WEINHEIM., pages 3213 - 3223, XP002593409, ISSN: 0009-2940 *
PICKENHAGEN W ET AL, HELVETICA CHIMICA ACTA, VERLAG HELVETICA CHIMICA ACTA, BASEL, CH LNKD- DOI:10.1002/HLCA.19840670405, vol. 67, 1 January 1984 (1984-01-01), pages 947 - 952, XP002120545, ISSN: 0018-019X *
R. W. HARTMANN ET AL.: "synthesis and evaluation of 17-aliphatic heterocycle-substituted steroidal inhibitors of 17alfa-hydroxylase/c17-20-lyase", JOURNAL OF MEDICINAL CHEMISTRY., vol. 43, no. 23, 2000, USAMERICAN CHEMICAL SOCIETY. WASHINGTON., pages 4437 - 4445, XP002593411, ISSN: 0022-2623 *
SNYDER H R ET AL: "THE SYNTHESIS OF AMINO MERCAPTANS FROM OLEFIN SULFIDES", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, NEW YORK, US LNKD- DOI:10.1021/JA01203A033, vol. 69, no. 11, 1 November 1947 (1947-11-01), pages 2672 - 2674, XP002049790, ISSN: 0002-7863 *
YUN GAO: "ti(o-i-pr)4-mediated formation of 2,3-epithio alcohols from 2,3-epoxy alcohols.", JOURNAL OF ORGANIC CHEMISTRY., vol. 53, 1988, USAMERICAN CHEMICAL SOCIETY. EASTON., pages 4114 - 4116, XP002593410, ISSN: 0022-3263 *

Also Published As

Publication number Publication date
GB2419593A (en) 2006-05-03
CA2524897A1 (en) 2004-11-25
ZA200508991B (en) 2007-07-25
EP1625106A2 (en) 2006-02-15
JP2007516956A (en) 2007-06-28
CN1925826A (en) 2007-03-07
AU2004238835A1 (en) 2004-11-25
GB0524992D0 (en) 2006-01-18
WO2004101472A2 (en) 2004-11-25
GB2419593B (en) 2007-10-10
KR20060032136A (en) 2006-04-14
WO2004101472A3 (en) 2006-11-23

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