ES2216757T3 - Ciclopentilalquilnitrilos yel uso de derivados de ciclopentilalquilo odoriferos como fragancias. - Google Patents
Ciclopentilalquilnitrilos yel uso de derivados de ciclopentilalquilo odoriferos como fragancias.Info
- Publication number
- ES2216757T3 ES2216757T3 ES00110015T ES00110015T ES2216757T3 ES 2216757 T3 ES2216757 T3 ES 2216757T3 ES 00110015 T ES00110015 T ES 00110015T ES 00110015 T ES00110015 T ES 00110015T ES 2216757 T3 ES2216757 T3 ES 2216757T3
- Authority
- ES
- Spain
- Prior art keywords
- cyclopentyl
- mmol
- solution
- yield
- oil
- 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.)
- Expired - Lifetime
Links
- 239000003205 fragrance Substances 0.000 title claims abstract description 15
- 150000001875 compounds Chemical class 0.000 claims abstract description 22
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 claims abstract description 6
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims abstract description 6
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- NVKDEKYWTQXNHG-UHFFFAOYSA-N 5-cyclopentylhexanenitrile Chemical compound N#CCCCC(C)C1CCCC1 NVKDEKYWTQXNHG-UHFFFAOYSA-N 0.000 claims description 8
- LHWCGANJGDSRAO-UHFFFAOYSA-N 5-cyclopentylhexanal Chemical compound O=CCCCC(C)C1CCCC1 LHWCGANJGDSRAO-UHFFFAOYSA-N 0.000 claims description 7
- WJFMFQSDFHVJDE-UHFFFAOYSA-N 4-cyclopentylpentanal Chemical compound O=CCCC(C)C1CCCC1 WJFMFQSDFHVJDE-UHFFFAOYSA-N 0.000 claims description 5
- DKNBYQDPXXREEZ-UHFFFAOYSA-N 5-(cyclopenten-1-yl)hexanenitrile Chemical compound N#CCCCC(C)C1=CCCC1 DKNBYQDPXXREEZ-UHFFFAOYSA-N 0.000 claims description 5
- PXBZLPOUZUBEKE-UHFFFAOYSA-N 5-cyclopentyl-3-methylpentanenitrile Chemical compound N#CCC(C)CCC1CCCC1 PXBZLPOUZUBEKE-UHFFFAOYSA-N 0.000 claims description 5
- IXZYGBIGKWQGGG-UHFFFAOYSA-N 5-cyclopentylidenehexanenitrile Chemical compound N#CCCCC(C)=C1CCCC1 IXZYGBIGKWQGGG-UHFFFAOYSA-N 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- DMYRODGWGFMICN-UHFFFAOYSA-N 4-cyclopentylpentanenitrile Chemical compound N#CCCC(C)C1CCCC1 DMYRODGWGFMICN-UHFFFAOYSA-N 0.000 claims description 4
- DYCQEQZZFFEORR-UHFFFAOYSA-N 5-cyclopentyl-3-methylpent-4-enal Chemical compound O=CCC(C)C=CC1CCCC1 DYCQEQZZFFEORR-UHFFFAOYSA-N 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 239000000203 mixture Substances 0.000 abstract description 29
- -1 and R2 is H Chemical group 0.000 abstract description 12
- 238000000034 method Methods 0.000 abstract description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 5
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 125000006193 alkinyl group Chemical group 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 description 32
- 230000035943 smell Effects 0.000 description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 25
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 24
- 238000005160 1H NMR spectroscopy Methods 0.000 description 23
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 18
- 239000003921 oil Substances 0.000 description 18
- 235000019198 oils Nutrition 0.000 description 18
- 239000012267 brine Substances 0.000 description 17
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 17
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 15
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 14
- 239000012074 organic phase Substances 0.000 description 14
- 238000003756 stirring Methods 0.000 description 14
- 239000011541 reaction mixture Substances 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 150000001299 aldehydes Chemical class 0.000 description 10
- 238000004821 distillation Methods 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 9
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 9
- 235000019341 magnesium sulphate Nutrition 0.000 description 9
- PQJPDBXYUUFDRK-UHFFFAOYSA-N 5-cyclopentylidenepentan-2-one Chemical compound CC(=O)CCC=C1CCCC1 PQJPDBXYUUFDRK-UHFFFAOYSA-N 0.000 description 8
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 8
- 229940022663 acetate Drugs 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 241000234435 Lilium Species 0.000 description 7
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 7
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- ZJCKWOJXOPMEIC-UHFFFAOYSA-N 4-cyclopentylpentanoic acid Chemical compound OC(=O)CCC(C)C1CCCC1 ZJCKWOJXOPMEIC-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000002304 perfume Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- HORKTQKYZDRBDC-UHFFFAOYSA-N 4-cyclopentylpentan-1-ol Chemical compound OCCCC(C)C1CCCC1 HORKTQKYZDRBDC-UHFFFAOYSA-N 0.000 description 5
- JKPGOFCUUPMORN-UHFFFAOYSA-N 5-cyclopentylhexan-1-ol Chemical compound OCCCCC(C)C1CCCC1 JKPGOFCUUPMORN-UHFFFAOYSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000005984 hydrogenation reaction Methods 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 4
- OKKSGXQZXUYTFN-UHFFFAOYSA-N 5-(cyclopenten-1-yl)-2-methylpentan-2-ol Chemical compound CC(C)(O)CCCC1=CCCC1 OKKSGXQZXUYTFN-UHFFFAOYSA-N 0.000 description 4
- UCPYATUXXKUYOR-UHFFFAOYSA-N 5-cyclopentyl-3-methylpent-4-en-1-ol Chemical compound OCCC(C)C=CC1CCCC1 UCPYATUXXKUYOR-UHFFFAOYSA-N 0.000 description 4
- AYQIQACXWFBWBQ-UHFFFAOYSA-N 5-cyclopentylidene-2-methylpentan-2-ol Chemical compound CC(C)(O)CCC=C1CCCC1 AYQIQACXWFBWBQ-UHFFFAOYSA-N 0.000 description 4
- FTFBMCDWXKVJQL-UHFFFAOYSA-N 5-cyclopentylpentan-2-ol Chemical compound CC(O)CCCC1CCCC1 FTFBMCDWXKVJQL-UHFFFAOYSA-N 0.000 description 4
- XJZVQSRSFLYZJW-UHFFFAOYSA-N 6-cyclopentyl-3-methylhexan-3-ol Chemical compound CCC(C)(O)CCCC1CCCC1 XJZVQSRSFLYZJW-UHFFFAOYSA-N 0.000 description 4
- WDYVUKGVKRZQNM-UHFFFAOYSA-N 6-phosphonohexylphosphonic acid Chemical compound OP(O)(=O)CCCCCCP(O)(O)=O WDYVUKGVKRZQNM-UHFFFAOYSA-N 0.000 description 4
- 240000007436 Cananga odorata Species 0.000 description 4
- 241000207199 Citrus Species 0.000 description 4
- 241001672694 Citrus reticulata Species 0.000 description 4
- 235000009046 Convallaria majalis Nutrition 0.000 description 4
- 244000068485 Convallaria majalis Species 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- 241000208152 Geranium Species 0.000 description 4
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 4
- 238000004587 chromatography analysis Methods 0.000 description 4
- 235000020971 citrus fruits Nutrition 0.000 description 4
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 4
- 239000002781 deodorant agent Substances 0.000 description 4
- 238000003795 desorption Methods 0.000 description 4
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 238000000746 purification Methods 0.000 description 4
- 239000012047 saturated solution Substances 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- KBSPSKDTOFIEFA-UHFFFAOYSA-N 5-(cyclopenten-1-yl)pentan-2-one Chemical compound CC(=O)CCCC1=CCCC1 KBSPSKDTOFIEFA-UHFFFAOYSA-N 0.000 description 3
- AMXANIUWWYEWKZ-UHFFFAOYSA-N 5-cyclopentyl-3-methylpentan-1-ol Chemical compound OCCC(C)CCC1CCCC1 AMXANIUWWYEWKZ-UHFFFAOYSA-N 0.000 description 3
- AJMGTRVUGVDVBN-UHFFFAOYSA-N 5-cyclopentyl-5-hydroxyhexanenitrile Chemical compound N#CCCCC(O)(C)C1CCCC1 AJMGTRVUGVDVBN-UHFFFAOYSA-N 0.000 description 3
- HEEHIVQCPHOLKN-UHFFFAOYSA-N 5-cyclopentylhexan-2-one Chemical compound CC(=O)CCC(C)C1CCCC1 HEEHIVQCPHOLKN-UHFFFAOYSA-N 0.000 description 3
- FCZJOXSWFLYEBQ-UHFFFAOYSA-N 5-cyclopentylidenepentan-2-ol Chemical compound CC(O)CCC=C1CCCC1 FCZJOXSWFLYEBQ-UHFFFAOYSA-N 0.000 description 3
- QQYHZGKDXBXAQZ-UHFFFAOYSA-N 5-cyclopentylpentan-2-one Chemical compound CC(=O)CCCC1CCCC1 QQYHZGKDXBXAQZ-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- 244000099147 Ananas comosus Species 0.000 description 3
- 235000007119 Ananas comosus Nutrition 0.000 description 3
- 235000007129 Cuminum cyminum Nutrition 0.000 description 3
- 244000304337 Cuminum cyminum Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- 235000012550 Pimpinella anisum Nutrition 0.000 description 3
- 240000004760 Pimpinella anisum Species 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 3
- 239000001926 citrus aurantium l. subsp. bergamia wright et arn. oil Substances 0.000 description 3
- CLXAUJXWXFEYTQ-UHFFFAOYSA-N ethyl 4-cyclopentylpentanoate Chemical compound CCOC(=O)CCC(C)C1CCCC1 CLXAUJXWXFEYTQ-UHFFFAOYSA-N 0.000 description 3
- 238000003818 flash chromatography Methods 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
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- 229930002839 ionone Natural products 0.000 description 3
- 150000002499 ionone derivatives Chemical class 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- LLRCQKLPJLNYLV-UHFFFAOYSA-N n-(5-cyclopentyl-3-methylpentylidene)hydroxylamine Chemical compound ON=CCC(C)CCC1CCCC1 LLRCQKLPJLNYLV-UHFFFAOYSA-N 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 235000017557 sodium bicarbonate Nutrition 0.000 description 3
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 2
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 2
- WINCSBAYCULVDU-UHFFFAOYSA-N 1,1,2-trimethylcyclopentane Chemical class CC1CCCC1(C)C WINCSBAYCULVDU-UHFFFAOYSA-N 0.000 description 2
- JSQRFMSSEXQLTC-UHFFFAOYSA-N 1-ethenylcyclopentan-1-ol Chemical compound C=CC1(O)CCCC1 JSQRFMSSEXQLTC-UHFFFAOYSA-N 0.000 description 2
- WNJSKZBEWNVKGU-UHFFFAOYSA-N 2,2-dimethoxyethylbenzene Chemical compound COC(OC)CC1=CC=CC=C1 WNJSKZBEWNVKGU-UHFFFAOYSA-N 0.000 description 2
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- BYPREWUYERMFNY-UHFFFAOYSA-N 5-(2-methylcyclopenten-1-yl)pentan-1-ol Chemical compound CC1=C(CCCCCO)CCC1 BYPREWUYERMFNY-UHFFFAOYSA-N 0.000 description 2
- YCHQVGKAXLCPGS-UHFFFAOYSA-N 5-(5-methylcyclopenten-1-yl)pentan-1-ol Chemical compound CC1CCC=C1CCCCCO YCHQVGKAXLCPGS-UHFFFAOYSA-N 0.000 description 2
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- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
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- VYLVYHXQOHJDJL-UHFFFAOYSA-K cerium trichloride Chemical compound Cl[Ce](Cl)Cl VYLVYHXQOHJDJL-UHFFFAOYSA-K 0.000 description 2
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- QNAQZOWKDCZUMY-UHFFFAOYSA-N ethyl 5-cyclopentyl-3-methylpent-4-enoate Chemical compound CCOC(=O)CC(C)C=CC1CCCC1 QNAQZOWKDCZUMY-UHFFFAOYSA-N 0.000 description 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
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- SDQFDHOLCGWZPU-UHFFFAOYSA-N lilial Chemical compound O=CC(C)CC1=CC=C(C(C)(C)C)C=C1 SDQFDHOLCGWZPU-UHFFFAOYSA-N 0.000 description 2
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- NXPHGHWWQRMDIA-UHFFFAOYSA-M magnesium;carbanide;bromide Chemical compound [CH3-].[Mg+2].[Br-] NXPHGHWWQRMDIA-UHFFFAOYSA-M 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
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- DTUQWGWMVIHBKE-UHFFFAOYSA-N phenylacetaldehyde Chemical compound O=CCC1=CC=CC=C1 DTUQWGWMVIHBKE-UHFFFAOYSA-N 0.000 description 2
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 2
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 2
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- 239000011630 iodine Substances 0.000 description 1
- 239000010656 jasmine oil Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000171 lavandula angustifolia l. flower oil Substances 0.000 description 1
- 239000001102 lavandula vera Substances 0.000 description 1
- 235000018219 lavender Nutrition 0.000 description 1
- UWKAYLJWKGQEPM-UHFFFAOYSA-N linalool acetate Natural products CC(C)=CCCC(C)(C=C)OC(C)=O UWKAYLJWKGQEPM-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000012280 lithium aluminium hydride Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229940041616 menthol Drugs 0.000 description 1
- RBAUBIIMPLZNGC-UHFFFAOYSA-N methyl 2-[[3-(4-tert-butylphenyl)-2-methylpropylidene]amino]benzoate Chemical compound COC(=O)C1=CC=CC=C1N=CC(C)CC1=CC=C(C(C)(C)C)C=C1 RBAUBIIMPLZNGC-UHFFFAOYSA-N 0.000 description 1
- YAHNYLGSSPTTAG-UHFFFAOYSA-N methyl n-(3,4-dichlorophenyl)carbamodithioate Chemical compound CSC(=S)NC1=CC=C(Cl)C(Cl)=C1 YAHNYLGSSPTTAG-UHFFFAOYSA-N 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000001702 nutmeg Substances 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- RUVINXPYWBROJD-UHFFFAOYSA-N para-methoxyphenyl Natural products COC1=CC=C(C=CC)C=C1 RUVINXPYWBROJD-UHFFFAOYSA-N 0.000 description 1
- LVECZGHBXXYWBO-UHFFFAOYSA-N pentadecanolide Natural products CC1CCCCCCCCCCCCC(=O)O1 LVECZGHBXXYWBO-UHFFFAOYSA-N 0.000 description 1
- 229940100595 phenylacetaldehyde Drugs 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
- WYVAMUWZEOHJOQ-UHFFFAOYSA-N propionic anhydride Chemical compound CCC(=O)OC(=O)CC WYVAMUWZEOHJOQ-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 235000019719 rose oil Nutrition 0.000 description 1
- 239000010666 rose oil Substances 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- CRDAMVZIKSXKFV-UHFFFAOYSA-N trans-Farnesol Natural products CC(C)=CCCC(C)=CCCC(C)=CCO CRDAMVZIKSXKFV-UHFFFAOYSA-N 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- DCSCXTJOXBUFGB-UHFFFAOYSA-N verbenone Natural products CC1=CC(=O)C2C(C)(C)C1C2 DCSCXTJOXBUFGB-UHFFFAOYSA-N 0.000 description 1
- WXETUDXXEZHSCS-MAVITOTKSA-N vertofix coeur Chemical compound C[C@@H]1CC[C@@]2(C(/CC3)=C\C(C)=O)[C@@H]3C(C)(C)[C@@H]1C2 WXETUDXXEZHSCS-MAVITOTKSA-N 0.000 description 1
- YEIGUXGHHKAURB-UHFFFAOYSA-N viridine Natural products O=C1C2=C3CCC(=O)C3=CC=C2C2(C)C(O)C(OC)C(=O)C3=COC1=C23 YEIGUXGHHKAURB-UHFFFAOYSA-N 0.000 description 1
- 239000008170 walnut oil Substances 0.000 description 1
- 229930007850 β-damascenone Natural products 0.000 description 1
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/31—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing rings other than six-membered aromatic rings
-
- 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
- C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
- C11B9/003—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing less than six carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/10—Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Polyurethanes Or Polyureas (AREA)
- Ceramic Products (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP99810585 | 1999-07-05 | ||
| EP99810585 | 1999-07-05 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2216757T3 true ES2216757T3 (es) | 2004-11-01 |
Family
ID=8242905
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES00110015T Expired - Lifetime ES2216757T3 (es) | 1999-07-05 | 2000-05-12 | Ciclopentilalquilnitrilos yel uso de derivados de ciclopentilalquilo odoriferos como fragancias. |
Country Status (11)
| Country | Link |
|---|---|
| US (3) | US6410000B1 (enExample) |
| JP (1) | JP2001048854A (enExample) |
| CN (1) | CN1147467C (enExample) |
| AT (1) | ATE263143T1 (enExample) |
| AU (1) | AU742027B2 (enExample) |
| BR (1) | BR0002448A (enExample) |
| CA (1) | CA2313337A1 (enExample) |
| DE (1) | DE60009394T2 (enExample) |
| ES (1) | ES2216757T3 (enExample) |
| SG (1) | SG109422A1 (enExample) |
| ZA (1) | ZA200002400B (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2579957A (en) * | 1947-10-30 | 1951-12-25 | Frederic A Pearne | Vacuum header for combine harvesters |
| GB0031047D0 (en) * | 2000-12-20 | 2001-01-31 | Quest Int | Perfume compositions |
| US7763238B2 (en) * | 2002-01-16 | 2010-07-27 | Monell Chemical Senses Center | Olfactory adaptation and cross-adapting agents to reduce the perception of body odors |
| JPWO2005087703A1 (ja) * | 2004-03-12 | 2008-01-24 | 日本ゼオン株式会社 | エステル化合物、香料組成物及びエステル化合物の製造方法 |
| KR100744823B1 (ko) * | 2006-02-15 | 2007-08-01 | 한국과학기술연구원 | (2-시클로펜테닐)클로로실란 유도체와 이의 제조방법 |
| MX2009006094A (es) * | 2006-12-08 | 2009-08-25 | Mane Fils V | Uso de derivados canfolenicos como ingredientes fragantes en perfumeria y saborizacion. |
| BR112013004077A2 (pt) * | 2010-08-25 | 2017-11-07 | Ramesh Vaze Kedar | composto, odorizante, fragância, composição de perfumaria, composto da fórmulai (i) aceitável pelo olfato e composição de perfumaria |
| FR2975283B1 (fr) * | 2011-05-17 | 2019-04-05 | V. Mane Fils | Utilisation sensorielle des derives du 6-cyclopentylidenehexane |
| GB201115409D0 (en) * | 2011-09-07 | 2011-10-19 | Givaudan Sa | Organic compounds |
| US9000226B2 (en) * | 2012-02-09 | 2015-04-07 | Firmenich Sa | Aldehydes as perfuming ingredients |
| WO2014103685A1 (ja) * | 2012-12-26 | 2014-07-03 | 花王株式会社 | ニトリル化合物 |
| US9643908B2 (en) * | 2013-09-06 | 2017-05-09 | Takasago International Corporation | Fragrance composition |
| ES3055109T3 (en) * | 2018-10-30 | 2026-02-10 | Firmenich & Cie | Cyclic oxy ether compounds as perfuming ingredients |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CS171102B1 (en) * | 1973-09-20 | 1976-10-31 | Ludvik Streinz | Insecticide and method of active substance preparationt |
| CH616077A5 (enExample) | 1976-06-30 | 1980-03-14 | Firmenich & Cie | |
| JPS55127316A (en) | 1979-03-26 | 1980-10-02 | Nippon Zeon Co Ltd | Perfume composition |
| GB2053199B (en) * | 1979-05-09 | 1983-07-06 | Polak S Frutal Work Bv | Nitriles and their use as perfume chemicals |
| EP0694520B1 (fr) | 1994-07-28 | 1999-10-06 | Firmenich Sa | Dérivés de l'aldéhyde campholénique et leur utilisation en parfumerie |
| EP0770671B1 (en) | 1995-11-03 | 1999-09-22 | Quest International B.V. | Cyclopentylidene-cyclopentanol in perfumery |
| JP3400291B2 (ja) * | 1996-09-17 | 2003-04-28 | 高砂香料工業株式会社 | （ｅ）−（ｒ）−２−アルキル−４−（２，２，３−トリメチルシクロペント−３−エン−１−イル）−２−ブテン−１−オール誘導体、その製造方法および用途 |
| EP0913383B1 (en) * | 1997-10-29 | 2001-09-05 | Givaudan SA | New spirocyclic compounds |
-
2000
- 2000-05-12 AT AT00110015T patent/ATE263143T1/de not_active IP Right Cessation
- 2000-05-12 ES ES00110015T patent/ES2216757T3/es not_active Expired - Lifetime
- 2000-05-12 DE DE60009394T patent/DE60009394T2/de not_active Expired - Lifetime
- 2000-05-16 ZA ZA200002400A patent/ZA200002400B/xx unknown
- 2000-05-31 SG SG200003033A patent/SG109422A1/en unknown
- 2000-06-06 AU AU37965/00A patent/AU742027B2/en not_active Ceased
- 2000-07-03 CN CNB001199293A patent/CN1147467C/zh not_active Expired - Fee Related
- 2000-07-04 JP JP2000201718A patent/JP2001048854A/ja active Pending
- 2000-07-04 CA CA002313337A patent/CA2313337A1/en not_active Abandoned
- 2000-07-05 US US09/609,845 patent/US6410000B1/en not_active Expired - Fee Related
- 2000-07-05 BR BR0002448-1A patent/BR0002448A/pt not_active IP Right Cessation
-
2001
- 2001-12-31 US US10/038,735 patent/US6399811B1/en not_active Expired - Fee Related
-
2002
- 2002-04-12 US US10/121,519 patent/US6441052B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CA2313337A1 (en) | 2001-01-05 |
| DE60009394D1 (de) | 2004-05-06 |
| US6410000B1 (en) | 2002-06-25 |
| US20020086901A1 (en) | 2002-07-04 |
| ZA200002400B (en) | 2000-11-16 |
| US6441052B1 (en) | 2002-08-27 |
| CN1290691A (zh) | 2001-04-11 |
| SG109422A1 (en) | 2005-03-30 |
| ATE263143T1 (de) | 2004-04-15 |
| CN1147467C (zh) | 2004-04-28 |
| JP2001048854A (ja) | 2001-02-20 |
| DE60009394T2 (de) | 2005-02-24 |
| US6399811B1 (en) | 2002-06-04 |
| AU3796500A (en) | 2001-04-26 |
| AU742027B2 (en) | 2001-12-13 |
| BR0002448A (pt) | 2001-03-13 |
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