JP2011503227A - パチュロール匂い物質 - Google Patents
パチュロール匂い物質 Download PDFInfo
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- JP2011503227A JP2011503227A JP2010534568A JP2010534568A JP2011503227A JP 2011503227 A JP2011503227 A JP 2011503227A JP 2010534568 A JP2010534568 A JP 2010534568A JP 2010534568 A JP2010534568 A JP 2010534568A JP 2011503227 A JP2011503227 A JP 2011503227A
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- perfume
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- 239000000126 substance Substances 0.000 title description 7
- GGHMUJBZYLPWFD-CUZKYEQNSA-N patchouli alcohol Chemical compound C1C[C@]2(C)[C@@]3(O)CC[C@H](C)[C@@H]2C[C@@H]1C3(C)C GGHMUJBZYLPWFD-CUZKYEQNSA-N 0.000 title description 3
- GGHMUJBZYLPWFD-UHFFFAOYSA-N rac-patchouli alcohol Natural products C1CC2(C)C3(O)CCC(C)C2CC1C3(C)C GGHMUJBZYLPWFD-UHFFFAOYSA-N 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims description 41
- 239000000203 mixture Substances 0.000 claims description 31
- 239000002304 perfume Substances 0.000 claims description 28
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- ZRCMFURZXFFPOG-UHFFFAOYSA-N 6,8,8a-trimethyl-2,3,4,4a,5,6,7,8-octahydro-1h-naphthalen-1-ol Chemical group OC1CCCC2CC(C)CC(C)C21C ZRCMFURZXFFPOG-UHFFFAOYSA-N 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 239000003599 detergent Substances 0.000 claims description 5
- 239000002671 adjuvant Substances 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 239000002386 air freshener Substances 0.000 claims description 3
- 239000004744 fabric Substances 0.000 claims description 3
- 239000002979 fabric softener Substances 0.000 claims description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 3
- 241000195940 Bryophyta Species 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 230000001166 anti-perspirative effect Effects 0.000 claims description 2
- 239000003213 antiperspirant Substances 0.000 claims description 2
- 239000007844 bleaching agent Substances 0.000 claims description 2
- 210000001072 colon Anatomy 0.000 claims description 2
- 239000002537 cosmetic Substances 0.000 claims description 2
- 239000002781 deodorant agent Substances 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 238000010409 ironing Methods 0.000 claims description 2
- 239000006210 lotion Substances 0.000 claims description 2
- 235000019341 magnesium sulphate Nutrition 0.000 claims description 2
- 235000011929 mousse Nutrition 0.000 claims description 2
- 235000019198 oils Nutrition 0.000 claims description 2
- 239000002453 shampoo Substances 0.000 claims description 2
- 239000000344 soap Substances 0.000 claims description 2
- 239000004753 textile Substances 0.000 claims description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L magnesium sulphate Substances [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 claims 1
- 239000004615 ingredient Substances 0.000 abstract description 11
- 235000019645 odor Nutrition 0.000 description 11
- 239000003205 fragrance Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- RZPFVRFSYMUDJO-UHFFFAOYSA-N 2h-naphthalen-1-one Chemical compound C1=CC=C2C(=O)CC=CC2=C1 RZPFVRFSYMUDJO-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- AFEFRXAPJRCTOW-UHFFFAOYSA-N 3,4,4a,5,6,7,8,8a-octahydro-2h-naphthalen-1-one Chemical compound C1CCCC2C(=O)CCCC21 AFEFRXAPJRCTOW-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- NDZOISQLWLWLEW-UHFFFAOYSA-N 1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalen-1-ol Chemical class C1CCCC2C(O)CCCC21 NDZOISQLWLWLEW-UHFFFAOYSA-N 0.000 description 3
- 241000222666 Boerhavia diffusa Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 235000011751 Pogostemon cablin Nutrition 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- 238000004821 distillation Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 238000007429 general method Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 230000001953 sensory effect Effects 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- -1 terpene hydrocarbons Chemical class 0.000 description 3
- HPCFPQXRRMYPAP-UHFFFAOYSA-N 6,8,8a-trimethyl-2,3,4,4a,5,6,7,8-octahydronaphthalen-1-one Chemical compound C1C(C)CC(C)C2(C)C1CCCC2=O HPCFPQXRRMYPAP-UHFFFAOYSA-N 0.000 description 2
- UFDDPEJEVXWZLN-UHFFFAOYSA-N 6,8,8a-trimethyl-2,3,4,4a,5,8-hexahydronaphthalen-1-one Chemical compound C1CCC(=O)C2(C)C(C)C=C(C)CC21 UFDDPEJEVXWZLN-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- SESFRYSPDFLNCH-UHFFFAOYSA-N benzyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OCC1=CC=CC=C1 SESFRYSPDFLNCH-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- 238000005354 coacervation Methods 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 238000010168 coupling process Methods 0.000 description 2
- 238000005859 coupling reaction Methods 0.000 description 2
- 150000001993 dienes Chemical class 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- 238000005538 encapsulation Methods 0.000 description 2
- 235000019439 ethyl acetate Nutrition 0.000 description 2
- 239000000796 flavoring agent Substances 0.000 description 2
- 235000019634 flavors Nutrition 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 1
- CJSBUWDGPXGFGA-UHFFFAOYSA-N 4-methylpenta-1,3-diene Chemical compound CC(C)=CC=C CJSBUWDGPXGFGA-UHFFFAOYSA-N 0.000 description 1
- 241000219495 Betulaceae Species 0.000 description 1
- MINMSMBTDGZVPU-UHFFFAOYSA-N CC1(CC2CCCC(C2(CC1)C)O)C Chemical compound CC1(CC2CCCC(C2(CC1)C)O)C MINMSMBTDGZVPU-UHFFFAOYSA-N 0.000 description 1
- OMPIYDSYGYKWSG-UHFFFAOYSA-N Citronensaeure-alpha-aethylester Natural products CCOC(=O)CC(O)(C(O)=O)CC(O)=O OMPIYDSYGYKWSG-UHFFFAOYSA-N 0.000 description 1
- 238000005698 Diels-Alder reaction Methods 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229910010082 LiAlH Inorganic materials 0.000 description 1
- 229920000881 Modified starch Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium on carbon Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- DOOTYTYQINUNNV-UHFFFAOYSA-N Triethyl citrate Chemical compound CCOC(=O)CC(O)(C(=O)OCC)CC(=O)OCC DOOTYTYQINUNNV-UHFFFAOYSA-N 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- VMWZRHGIAVCFNS-UHFFFAOYSA-J aluminum;lithium;tetrahydroxide Chemical compound [Li+].[OH-].[OH-].[OH-].[OH-].[Al+3] VMWZRHGIAVCFNS-UHFFFAOYSA-J 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229960002903 benzyl benzoate Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000000306 component Substances 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical class OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 150000002016 disaccharides Chemical class 0.000 description 1
- 238000004851 dishwashing Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000010828 elution Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940057975 ethyl citrate Drugs 0.000 description 1
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000000416 hydrocolloid Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019426 modified starch Nutrition 0.000 description 1
- 150000002772 monosaccharides Chemical class 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000008786 sensory perception of smell Effects 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 230000004936 stimulating effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 235000013769 triethyl citrate Nutrition 0.000 description 1
- 150000004043 trisaccharides Chemical class 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002936 woody odorant Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/22—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system
- C07C35/23—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with hydroxy on a condensed ring system having two rings
- C07C35/36—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring polycyclic, at least one hydroxy group bound to a condensed ring system with hydroxy on a condensed ring system having two rings the condensed ring system being a (4.4.0) system, e.g. naphols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/013—Esters of alcohols having the esterified hydroxy group bound to a carbon atom of a ring other than a six-membered aromatic ring
-
- 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
- C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
- C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings
- C11B9/0049—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms
- C11B9/0053—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms both rings being six-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/14—All rings being cycloaliphatic
- C07C2602/26—All rings being cycloaliphatic the ring system containing ten carbon atoms
- C07C2602/28—Hydrogenated naphthalenes
Abstract
Description
我々の知識の及ぶ限りでは、本発明の化合物は新しく、かつ付香成分として公知である近い構造類似体を有さない。
驚くべきことに、式(I)
R2は、メチル基又はエチル基を示し、かつ
それぞれのRは、互いに独立して、水素原子又はメチル基を示し、及び少なくとも2つの該Rはメチル基である]で示される化合物が、例えばウッディー−アーシータイプの匂いノートを付与するための付香成分として使用されうることが、今日発見されている。
i)付香成分として、前記のような少なくとも1つの本発明の化合物、
ii)香料キャリヤー及び香料ベースからなる群から選択される少なくとも1つの成分、並びに
iii)場合により少なくとも1つの香料補助剤
を含有する付香組成物である。
i)付香成分として、少なくとも1つの前記のような式(I)の化合物、又は本発明の付香組成物、及び
ii)消費製品ベース
を含有する着香物品が、本発明の目的でもある。
本発明は、次の実施例の方法によってさらに詳細に記載され、その際、略語は当該技術分野において通常の意味を有し、温度を摂氏度(℃)で表し、NMRスペクトルデータを、CDCl3中で(別の方法で安定しない場合に)360又は400MHz機械を用いて1H及び13Cとして記録し、化学シフト(chemical displacement)δを、標準としてのTMSに対してppmで表し、結合定数Jを、Hzで表す。
ペルヒドロ−6,8,8a−トリメチル−1−ナフタレノールの合成
I)ディールス−アルダー結合のための一般的な方法
500mlの反応器中に、AlEtCl2、又はAlCl3、BHT0.1g及びトルエン、又はCH2Cl2を導入した。そして、激しい撹拌下で、温度30℃未満を維持するように、適切なシクロヘキサノンを滴下して添加した。その後、ジエンを滴下して添加し、そして、反応が終了した場合に、その反応混合物を、5%HCl水で加水分解し、Et2Oで2回抽出した。その有機層を、飽和NaHCO3水溶液、水、食塩水で洗浄し、そしてNa2SO4で乾燥した。その溶剤の蒸発、クロマトグラフィー(SiO2、溶出ヘプタン/AcOEt 98:2)、及び蒸留は、不飽和ナフタレノンを提供した。
100mlフラスコ中に、適切な不飽和ナフタレノン、エチルアセテート、及び不飽和ナフタレノンに対してPd/C 5%の10%(w/w)を導入した。そして、その混合物を、H2下で、室温で、水素の理論量を消費するまで撹拌した。その後、その反応混合物を、Nylon6/6で濾過した。溶液の蒸発及び蒸留は、ペルヒドロナフタレノンを提供した。
Ar雰囲気下で維持された100mlフラスコ中に、ケトンに対して、Et2O中でLiAlH4の2モーラー当量を導入した。そして適切なペルヒドロナフタレノンを、還流を維持するように、滴下して添加した。反応の完了後に、その混合物を、30分間還流で撹拌した。その後、該反応混合物を、NaOH水の化学量論量で加水分解し、そしてその有機層を、Na2SO4で乾燥した。溶剤の蒸発及び蒸留は、ペルヒドロナフタレノールを提供した。
一般の製造方法I)によって製造して、次の量を有した:
2−メチル−2−シクロヘキサン−1−オン(22g;0.2mol)
エチルアルミニウムジクロリド(ヘキサン中で1モーラー溶液;40ml;0.04mol)
メチルペンタジエン(24.6g;0.3mol)、ジクロロメタン(200ml)。
一般の製造方法II)によって製造して、次の量を有した:
6,8,8a−トリメチル−3,4,4a、5,8,8a−ヘキサヒドロ−1(2H)−ナフタレノン(9.60g:0.05mol)
5%Pd−C(1.0g)、EtOAc(100ml)。
一般の製造方法III)によって製造して、次の量を有した:
ペルヒドロ−6,8,8a−トリメチル−1−ナフタレノン(3g;0.016mmol)
リチウムアルミニウム水酸化物(0.31g;0.008mol)、ジエチルエーテル(30ml)。
Claims (7)
- ペルヒドロ−6,8,8a−トリメチル−1−ナフタレノールであることを特徴とする、請求項1に記載の化合物。
- 以下、
i)請求項1、2又は3のいずれか1項に記載の少なくとも1つの本発明の化合物、
ii)香料キャリヤー及び香料ベースからなる群から選択される少なくとも1つの成分、並びに
iii)場合により少なくとも1つの香料補助剤
を含有する付香組成物。 - 以下、
i)請求項1、2もしくは3のいずれか1項に記載の少なくとも1つの式(I)の化合物、又は請求項4に記載の組成物、及び
ii)消費製品ベース
を含有する着香物品。 - 前記消費製品ベースが、固体もしくは液体の洗剤、織物柔軟剤、香水、コロンもしくはアフターシェイブローション、香水石鹸、シャワーもしくはバスソルト、ムース、オイルもしくはゲル、衛生製品、ヘアケア製品、シャンプー、ボディケア製品、消臭剤もしくは制汗剤、エアーフレッシュナー、化粧品、織物回復剤、アイロン水、紙、ふき取りクロス又は漂白剤であることを特徴とする、請求項5に記載の着香物品。
- 請求項1、2又は3のいずれか1項に記載の化合物の付香成分としての使用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IBPCT/IB2007/054690 | 2007-11-19 | ||
IB2007054690 | 2007-11-19 | ||
PCT/IB2008/054491 WO2009066193A1 (en) | 2007-11-19 | 2008-10-29 | Patchoulol odorant |
Publications (2)
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JP2011503227A true JP2011503227A (ja) | 2011-01-27 |
JP5431350B2 JP5431350B2 (ja) | 2014-03-05 |
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ID=40348003
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JP2010534568A Expired - Fee Related JP5431350B2 (ja) | 2007-11-19 | 2008-10-29 | パチュロール匂い物質 |
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US (1) | US7973200B2 (ja) |
EP (1) | EP2212271B1 (ja) |
JP (1) | JP5431350B2 (ja) |
CN (1) | CN101861296B (ja) |
BR (1) | BRPI0817987A2 (ja) |
ES (1) | ES2401749T3 (ja) |
IL (1) | IL205805A (ja) |
WO (1) | WO2009066193A1 (ja) |
Cited By (1)
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JP2014529333A (ja) * | 2011-07-07 | 2014-11-06 | フイルメニツヒ ソシエテ アノニムFirmenich Sa | アロマティックノートを有するペンタ/ヘキサメチル−3,4,5,8−テトラヒドロ−1(2h)−ナフタレノン誘導体 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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EP2687586B1 (de) | 2012-07-17 | 2016-11-23 | Symrise AG | Verwendung definierter Cyclohexenone als Mittel zum überadditiven Verstärken eines Geruchseindrucks sowie Riech- und/oder Geschmacksstoffkomposition |
GB201516911D0 (en) * | 2015-09-24 | 2015-11-11 | Givaudan Sa | Perfume compositions |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
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US4339467A (en) | 1980-08-29 | 1982-07-13 | International Flavors & Fragrances Inc. | Flavoring with methyl substituted oxobicyclo-4,4,0-decane derivatives |
EP0167709B1 (fr) | 1984-07-12 | 1989-12-06 | Firmenich Sa | 1,2,3,4,4a,5,8a-Octahydro-2,2,6,8-tétraméthyl-1-naphtalénol, son utilisation en tant qu'ingrédient parfumant et procédé pour sa préparation |
EP0882697B1 (fr) * | 1997-06-06 | 2001-10-04 | Firmenich Sa | Composés parfumants à odeur boisée, fruitée |
US7378383B2 (en) * | 2004-06-08 | 2008-05-27 | Firmenich Sa | Perfuming ingredients of the woody type |
EP1605035B1 (en) | 2004-06-08 | 2007-09-19 | Firmenich Sa | Perfuming ingredients of the woody type |
JP2009500467A (ja) * | 2005-07-01 | 2009-01-08 | フイルメニツヒ ソシエテ アノニム | ウッディータイプの付香成分 |
-
2008
- 2008-10-29 ES ES08852334T patent/ES2401749T3/es active Active
- 2008-10-29 WO PCT/IB2008/054491 patent/WO2009066193A1/en active Application Filing
- 2008-10-29 EP EP08852334A patent/EP2212271B1/en active Active
- 2008-10-29 BR BRPI0817987-5A patent/BRPI0817987A2/pt not_active IP Right Cessation
- 2008-10-29 CN CN2008801164196A patent/CN101861296B/zh active Active
- 2008-10-29 US US12/738,737 patent/US7973200B2/en active Active
- 2008-10-29 JP JP2010534568A patent/JP5431350B2/ja not_active Expired - Fee Related
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JP2014529333A (ja) * | 2011-07-07 | 2014-11-06 | フイルメニツヒ ソシエテ アノニムFirmenich Sa | アロマティックノートを有するペンタ/ヘキサメチル−3,4,5,8−テトラヒドロ−1(2h)−ナフタレノン誘導体 |
Also Published As
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JP5431350B2 (ja) | 2014-03-05 |
ES2401749T3 (es) | 2013-04-24 |
US7973200B2 (en) | 2011-07-05 |
US20100209372A1 (en) | 2010-08-19 |
BRPI0817987A2 (pt) | 2015-04-07 |
IL205805A0 (en) | 2010-11-30 |
CN101861296A (zh) | 2010-10-13 |
EP2212271B1 (en) | 2013-01-09 |
CN101861296B (zh) | 2013-05-01 |
EP2212271A1 (en) | 2010-08-04 |
IL205805A (en) | 2014-03-31 |
WO2009066193A1 (en) | 2009-05-28 |
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