KR20070006895A - 지환식 카복실산 옥시카본일메틸 에스터 및 이의취기제로서의 용도 - Google Patents
지환식 카복실산 옥시카본일메틸 에스터 및 이의취기제로서의 용도 Download PDFInfo
- Publication number
- KR20070006895A KR20070006895A KR1020067023223A KR20067023223A KR20070006895A KR 20070006895 A KR20070006895 A KR 20070006895A KR 1020067023223 A KR1020067023223 A KR 1020067023223A KR 20067023223 A KR20067023223 A KR 20067023223A KR 20070006895 A KR20070006895 A KR 20070006895A
- Authority
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- South Korea
- Prior art keywords
- ester
- carboxylic acid
- octane
- formula
- compound
- 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- Withdrawn
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- -1 Alicyclic Carboxylic Acid Oxycarbonylmethyl Esters Chemical class 0.000 title abstract description 13
- 239000003795 chemical substances by application Substances 0.000 title description 2
- 239000003205 fragrance Substances 0.000 claims abstract description 31
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 14
- 239000002304 perfume Substances 0.000 claims description 14
- SFDDJGIMHONNHU-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 2-(3,3-dimethylcyclohexyl)propanoate Chemical compound CCOC(=O)COC(=O)C(C)C1CCCC(C)(C)C1 SFDDJGIMHONNHU-UHFFFAOYSA-N 0.000 claims description 7
- 238000000034 method Methods 0.000 claims description 7
- JHIRZNSVBGSOFD-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 2,7,7-trimethylspiro[2.5]octane-2-carboxylate Chemical compound CCOC(=O)COC(=O)C1(C)CC11CC(C)(C)CCC1 JHIRZNSVBGSOFD-UHFFFAOYSA-N 0.000 claims description 3
- 239000002537 cosmetic Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- JKRGTFRNUAEIHZ-UHFFFAOYSA-N (2-cyclopropyloxy-2-oxoethyl) 2,7,7-trimethylspiro[2.5]octane-2-carboxylate Chemical compound C1CC1OC(=O)COC(=O)C1(C)CC11CCCC(C)(C)C1 JKRGTFRNUAEIHZ-UHFFFAOYSA-N 0.000 claims 1
- PPXXHLDZUPHDFL-UHFFFAOYSA-N (2-cyclopropyloxy-2-oxoethyl) 2,7-dimethylspiro[2.5]octane-2-carboxylate Chemical compound C1C(C)CCCC11C(C(=O)OCC(=O)OC2CC2)(C)C1 PPXXHLDZUPHDFL-UHFFFAOYSA-N 0.000 claims 1
- HDCMFDOJLHAMLU-UHFFFAOYSA-N (2-cyclopropyloxy-2-oxoethyl) 2-(3,3-dimethylcyclohexyl)propanoate Chemical compound C1CC1OC(=O)COC(=O)C(C)C1CCCC(C)(C)C1 HDCMFDOJLHAMLU-UHFFFAOYSA-N 0.000 claims 1
- MLCSSGRQSXZLHZ-UHFFFAOYSA-N (2-cyclopropyloxy-2-oxoethyl) 2-(3-methylcyclohexyl)propanoate Chemical compound C1CC1OC(=O)COC(=O)C(C)C1CCCC(C)C1 MLCSSGRQSXZLHZ-UHFFFAOYSA-N 0.000 claims 1
- REKFLIURODXBEK-UHFFFAOYSA-N (2-cyclopropyloxy-2-oxoethyl) 2-cyclohexylpropanoate Chemical compound C1CC1OC(=O)COC(=O)C(C)C1CCCCC1 REKFLIURODXBEK-UHFFFAOYSA-N 0.000 claims 1
- DPAIXEQPNMQLJQ-UHFFFAOYSA-N (2-cyclopropyloxy-2-oxoethyl) 2-methylspiro[2.5]octane-2-carboxylate Chemical compound C1CC1OC(=O)COC(=O)C1(C)CC11CCCCC1 DPAIXEQPNMQLJQ-UHFFFAOYSA-N 0.000 claims 1
- UGEBBCSDCVVJSD-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 2,7-dimethylspiro[2.5]octane-2-carboxylate Chemical compound CCOC(=O)COC(=O)C1(C)CC11CC(C)CCC1 UGEBBCSDCVVJSD-UHFFFAOYSA-N 0.000 claims 1
- OYQUOZKFLPVLKQ-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 2-(3-methylcyclohexyl)propanoate Chemical compound CCOC(=O)COC(=O)C(C)C1CCCC(C)C1 OYQUOZKFLPVLKQ-UHFFFAOYSA-N 0.000 claims 1
- RZMYWFNMHVTNLI-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 2-cyclohexylpropanoate Chemical compound CCOC(=O)COC(=O)C(C)C1CCCCC1 RZMYWFNMHVTNLI-UHFFFAOYSA-N 0.000 claims 1
- AFZZHFUARFGHFH-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 2-methylspiro[2.5]octane-2-carboxylate Chemical compound CCOC(=O)COC(=O)C1(C)CC11CCCCC1 AFZZHFUARFGHFH-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 238000003756 stirring Methods 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 9
- 239000000284 extract Substances 0.000 description 7
- 238000010992 reflux Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 241000402754 Erythranthe moschata Species 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
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- 239000000047 product 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
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- 239000002244 precipitate Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- PSSKAIMYKSRYIQ-UHFFFAOYSA-N ethyl 2-(3,3-dimethylcyclohexylidene)propanoate Chemical compound CCOC(=O)C(C)=C1CCCC(C)(C)C1 PSSKAIMYKSRYIQ-UHFFFAOYSA-N 0.000 description 3
- BVSRWCMAJISCTD-UHFFFAOYSA-N ethyl 2-diethoxyphosphorylpropanoate Chemical compound CCOC(=O)C(C)P(=O)(OCC)OCC BVSRWCMAJISCTD-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 150000002596 lactones Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000000741 silica gel Substances 0.000 description 3
- 229910002027 silica gel Inorganic materials 0.000 description 3
- 229960001866 silicon dioxide Drugs 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000003828 vacuum filtration Methods 0.000 description 3
- 238000001644 13C nuclear magnetic resonance spectroscopy Methods 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- MMTRVRVLQXOINK-UHFFFAOYSA-N 2,7,7-trimethylspiro[2.5]octane-2-carboxylic acid Chemical compound OC(=O)C1(C)CC11CC(C)(C)CCC1 MMTRVRVLQXOINK-UHFFFAOYSA-N 0.000 description 2
- ZDNDDXBTIZOZDR-UHFFFAOYSA-N 2-(3,3-dimethylcyclohexylidene)propanoic acid Chemical compound OC(=O)C(C)=C1CCCC(C)(C)C1 ZDNDDXBTIZOZDR-UHFFFAOYSA-N 0.000 description 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
- XPCTZQVDEJYUGT-UHFFFAOYSA-N 3-hydroxy-2-methyl-4-pyrone Chemical compound CC=1OC=CC(=O)C=1O XPCTZQVDEJYUGT-UHFFFAOYSA-N 0.000 description 2
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 2
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QUKGYYKBILRGFE-UHFFFAOYSA-N benzyl acetate Chemical compound CC(=O)OCC1=CC=CC=C1 QUKGYYKBILRGFE-UHFFFAOYSA-N 0.000 description 2
- 239000012267 brine Substances 0.000 description 2
- HQKQRXZEXPXXIG-VJOHVRBBSA-N chembl2333940 Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@H]1[C@@](OC(C)=O)(C)CC2 HQKQRXZEXPXXIG-VJOHVRBBSA-N 0.000 description 2
- QMVPMAAFGQKVCJ-UHFFFAOYSA-N citronellol Chemical compound OCCC(C)CCC=C(C)C QMVPMAAFGQKVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- YZAFURQSICZZHZ-UHFFFAOYSA-N ethyl 2,7,7-trimethylspiro[2.5]octane-2-carboxylate Chemical compound CCOC(=O)C1(C)CC11CC(C)(C)CCC1 YZAFURQSICZZHZ-UHFFFAOYSA-N 0.000 description 2
- ZANNOFHADGWOLI-UHFFFAOYSA-N ethyl 2-hydroxyacetate Chemical compound CCOC(=O)CO ZANNOFHADGWOLI-UHFFFAOYSA-N 0.000 description 2
- RRAFCDWBNXTKKO-UHFFFAOYSA-N eugenol Chemical compound COC1=CC(CC=C)=CC=C1O RRAFCDWBNXTKKO-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 150000002678 macrocyclic compounds Chemical class 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
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- 239000012044 organic layer Substances 0.000 description 2
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- CZCBTSFUTPZVKJ-UHFFFAOYSA-N rose oxide Chemical compound CC1CCOC(C=C(C)C)C1 CZCBTSFUTPZVKJ-UHFFFAOYSA-N 0.000 description 2
- 238000007127 saponification reaction Methods 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
- LFSYLMRHJKGLDV-UHFFFAOYSA-N tetradecanolide Natural products O=C1CCCCCCCCCCCCCO1 LFSYLMRHJKGLDV-UHFFFAOYSA-N 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- PHXATPHONSXBIL-UHFFFAOYSA-N xi-gamma-Undecalactone Chemical compound CCCCCCCC1CCC(=O)O1 PHXATPHONSXBIL-UHFFFAOYSA-N 0.000 description 2
- ORHSGDMSYGKJJY-SAIIYOCFSA-N (1'r,6's)-2,2,4',7',7'-pentamethylspiro[1,3-dioxane-5,5'-bicyclo[4.1.0]heptane] Chemical compound C12([C@H]3[C@H](C3(C)C)CCC2C)COC(C)(C)OC1 ORHSGDMSYGKJJY-SAIIYOCFSA-N 0.000 description 1
- SMUBYRSPILIFEE-UHFFFAOYSA-N (2-ethoxy-2-oxoethyl) 2-(3,3-dimethylcyclohexylidene)propanoate Chemical compound CCOC(=O)COC(=O)C(C)=C1CCCC(C)(C)C1 SMUBYRSPILIFEE-UHFFFAOYSA-N 0.000 description 1
- AVJMJMPVWWWELJ-DHZHZOJOSA-N (2e)-1-methoxy-3,7-dimethylocta-2,6-diene Chemical compound COC\C=C(/C)CCC=C(C)C AVJMJMPVWWWELJ-DHZHZOJOSA-N 0.000 description 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- QMVPMAAFGQKVCJ-SNVBAGLBSA-N (R)-(+)-citronellol Natural products OCC[C@H](C)CCC=C(C)C QMVPMAAFGQKVCJ-SNVBAGLBSA-N 0.000 description 1
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
- BVDMQAQCEBGIJR-UHFFFAOYSA-N 1-(2,2,6-trimethylcyclohexyl)hexan-3-ol Chemical compound CCCC(O)CCC1C(C)CCCC1(C)C BVDMQAQCEBGIJR-UHFFFAOYSA-N 0.000 description 1
- VPKMGDRERYMTJX-CMDGGOBGSA-N 1-(2,6,6-Trimethyl-2-cyclohexen-1-yl)-1-penten-3-one Chemical compound CCC(=O)\C=C\C1C(C)=CCCC1(C)C VPKMGDRERYMTJX-CMDGGOBGSA-N 0.000 description 1
- HMKKIXGYKWDQSV-SDNWHVSQSA-N 2-Pentyl-3-phenyl-2-propenal Chemical compound CCCCC\C(C=O)=C/C1=CC=CC=C1 HMKKIXGYKWDQSV-SDNWHVSQSA-N 0.000 description 1
- VRLUSLNMNQAPOH-UHFFFAOYSA-N 2-cyclohexylpropanoic acid Chemical class OC(=O)C(C)C1CCCCC1 VRLUSLNMNQAPOH-UHFFFAOYSA-N 0.000 description 1
- ZVJQBBYAVPAFLX-UHFFFAOYSA-N 3,3-dimethylcyclohexan-1-one Chemical compound CC1(C)CCCC(=O)C1 ZVJQBBYAVPAFLX-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
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- 241000499489 Castor canadensis Species 0.000 description 1
- NPBVQXIMTZKSBA-UHFFFAOYSA-N Chavibetol Natural products COC1=CC=C(CC=C)C=C1O NPBVQXIMTZKSBA-UHFFFAOYSA-N 0.000 description 1
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- XRHCAGNSDHCHFJ-UHFFFAOYSA-N Ethylene brassylate Chemical compound O=C1CCCCCCCCCCCC(=O)OCCO1 XRHCAGNSDHCHFJ-UHFFFAOYSA-N 0.000 description 1
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- AEMRFAOFKBGASW-UHFFFAOYSA-M Glycolate Chemical compound OCC([O-])=O AEMRFAOFKBGASW-UHFFFAOYSA-M 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
- 238000006546 Horner-Wadsworth-Emmons reaction Methods 0.000 description 1
- 235000010254 Jasminum officinale Nutrition 0.000 description 1
- 240000005385 Jasminum sambac Species 0.000 description 1
- 238000000023 Kugelrohr distillation Methods 0.000 description 1
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- 235000011779 Menyanthes trifoliata Nutrition 0.000 description 1
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- YPZUZOLGGMJZJO-UHFFFAOYSA-N ambrofix Natural products C1CC2C(C)(C)CCCC2(C)C2C1(C)OCC2 YPZUZOLGGMJZJO-UHFFFAOYSA-N 0.000 description 1
- YPZUZOLGGMJZJO-LQKXBSAESA-N ambroxan Chemical compound CC([C@@H]1CC2)(C)CCC[C@]1(C)[C@@H]1[C@]2(C)OCC1 YPZUZOLGGMJZJO-LQKXBSAESA-N 0.000 description 1
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- 239000012876 carrier material Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
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- 238000006731 degradation reaction Methods 0.000 description 1
- SQIFACVGCPWBQZ-UHFFFAOYSA-N delta-terpineol Natural products CC(C)(O)C1CCC(=C)CC1 SQIFACVGCPWBQZ-UHFFFAOYSA-N 0.000 description 1
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- 230000000694 effects Effects 0.000 description 1
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- 235000019634 flavors Nutrition 0.000 description 1
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- PHXATPHONSXBIL-JTQLQIEISA-N gamma-Undecalactone Natural products CCCCCCC[C@H]1CCC(=O)O1 PHXATPHONSXBIL-JTQLQIEISA-N 0.000 description 1
- 229940020436 gamma-undecalactone Drugs 0.000 description 1
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- KVWWIYGFBYDJQC-UHFFFAOYSA-N methyl dihydrojasmonate Chemical compound CCCCCC1C(CC(=O)OC)CCC1=O KVWWIYGFBYDJQC-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
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- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
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- 229920000642 polymer Polymers 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
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- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- GOZDTZWAMGHLDY-UHFFFAOYSA-L sodium picosulfate Chemical compound [Na+].[Na+].C1=CC(OS(=O)(=O)[O-])=CC=C1C(C=1N=CC=CC=1)C1=CC=C(OS([O-])(=O)=O)C=C1 GOZDTZWAMGHLDY-UHFFFAOYSA-L 0.000 description 1
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- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- 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
- C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/753—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring of polycyclic acids
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/50—Spiro compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0410134.1A GB0410134D0 (en) | 2004-05-07 | 2004-05-07 | Organic compounds |
| GB0410134.1 | 2004-05-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20070006895A true KR20070006895A (ko) | 2007-01-11 |
Family
ID=32482789
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020067023223A Withdrawn KR20070006895A (ko) | 2004-05-07 | 2005-05-04 | 지환식 카복실산 옥시카본일메틸 에스터 및 이의취기제로서의 용도 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US7687452B2 (enExample) |
| EP (1) | EP1743013B1 (enExample) |
| JP (1) | JP2007536285A (enExample) |
| KR (1) | KR20070006895A (enExample) |
| CN (1) | CN1950490A (enExample) |
| AT (1) | ATE381605T1 (enExample) |
| BR (1) | BRPI0509666A (enExample) |
| DE (1) | DE602005003937T2 (enExample) |
| ES (1) | ES2297694T3 (enExample) |
| GB (1) | GB0410134D0 (enExample) |
| MX (1) | MXPA06012767A (enExample) |
| WO (1) | WO2005108534A1 (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1842564B1 (en) * | 2006-04-05 | 2014-02-19 | The Procter and Gamble Company | Absorbent articles including odour control system |
| US8835511B2 (en) * | 2007-04-04 | 2014-09-16 | The Procter & Gamble Company | Absorbent articles including an odor control system |
| JP5442356B2 (ja) * | 2009-08-11 | 2014-03-12 | 長谷川香料株式会社 | 脂肪族エステル類、該化合物を含有する香料組成物および該化合物の製造法 |
| US8846723B2 (en) | 2010-07-29 | 2014-09-30 | Eastman Chemical Company | Esters of O-substituted hydroxy carboxylic acids and preparations thereof |
| US8613940B2 (en) | 2010-09-03 | 2013-12-24 | Eastman Chemical Company | Carbonate derivatives as skin care |
| US8329938B2 (en) | 2011-02-21 | 2012-12-11 | Eastman Chemical Company | Hydroxyalkanoic acid and hydroxyalkanoice acid oligomer esters of retinol |
| EP3135663B1 (en) | 2014-04-21 | 2019-02-27 | Takasago International Corporation | Novel compound, and flavor composition containing said compound |
| PL234189B1 (pl) * | 2017-12-01 | 2020-01-31 | Politechnika Wroclawska | (2E)-2-[(2S,5R)-5-metylo-2-(propan-2-ylo)cykloheksylideno]butanian etylu i sposób jego wytwarzania |
| EP3730476B1 (en) | 2017-12-22 | 2022-07-20 | Takasago International Corporation | Compound having musk-like scent and perfume composition containing same |
| WO2024206466A1 (en) | 2023-03-30 | 2024-10-03 | International Flavors & Fragrances Inc. | Method for producing a musk fragrance intermediate using copper catalysts |
| CN118834120A (zh) | 2023-04-11 | 2024-10-25 | 国际香料和香精公司 | 使用AlCl3作为催化剂的用于制备麝香香精中间体的方法 |
| WO2025238055A1 (en) | 2024-05-15 | 2025-11-20 | International Flavors & Fragrances Inc. | Method for producing a musk fragrance intermediate using heterogeneous catalysts |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0749593B2 (ja) * | 1989-07-28 | 1995-05-31 | 花王株式会社 | ２―シクロヘキシルプロピオン酸またはその誘導体を含有する調合香料組成物 |
| US5166412A (en) * | 1990-08-28 | 1992-11-24 | Firmenich S.A. | Esters and their use in perfumery |
| JPH07310089A (ja) * | 1994-05-19 | 1995-11-28 | Ogawa Koryo Kk | １−オキサスピロ（２．５）オクタン−２−カルボン酸エステルからなる香料 |
| US6384269B1 (en) * | 1999-08-25 | 2002-05-07 | Firmenich Sa | Esters with musky odor and their use in perfumery |
| CN1153758C (zh) * | 1998-09-09 | 2004-06-16 | 弗门尼舍有限公司 | 具有麝香气味的酯类及其香料用途 |
| EP1182190A1 (en) * | 2000-08-25 | 2002-02-27 | Givaudan SA | Unsaturated esters |
| EP1262474A1 (en) * | 2001-06-01 | 2002-12-04 | Givaudan SA | Cycloalkanecarboxylic acid derivatives as fragrants with musk characteristics |
| GB0227807D0 (en) | 2002-11-29 | 2003-01-08 | Givaudan Sa | Improvements in or relating ot organic compounds |
-
2004
- 2004-05-07 GB GBGB0410134.1A patent/GB0410134D0/en not_active Ceased
-
2005
- 2005-05-04 BR BRPI0509666-9A patent/BRPI0509666A/pt not_active IP Right Cessation
- 2005-05-04 WO PCT/CH2005/000251 patent/WO2005108534A1/en not_active Ceased
- 2005-05-04 EP EP05732413A patent/EP1743013B1/en not_active Expired - Lifetime
- 2005-05-04 JP JP2007511828A patent/JP2007536285A/ja not_active Ceased
- 2005-05-04 US US11/568,475 patent/US7687452B2/en not_active Expired - Fee Related
- 2005-05-04 KR KR1020067023223A patent/KR20070006895A/ko not_active Withdrawn
- 2005-05-04 DE DE602005003937T patent/DE602005003937T2/de not_active Expired - Lifetime
- 2005-05-04 AT AT05732413T patent/ATE381605T1/de not_active IP Right Cessation
- 2005-05-04 ES ES05732413T patent/ES2297694T3/es not_active Expired - Lifetime
- 2005-05-04 CN CNA2005800146426A patent/CN1950490A/zh active Pending
- 2005-05-04 MX MXPA06012767A patent/MXPA06012767A/es active IP Right Grant
Also Published As
| Publication number | Publication date |
|---|---|
| US20070225201A1 (en) | 2007-09-27 |
| JP2007536285A (ja) | 2007-12-13 |
| ATE381605T1 (de) | 2008-01-15 |
| ES2297694T3 (es) | 2008-05-01 |
| DE602005003937D1 (de) | 2008-01-31 |
| BRPI0509666A (pt) | 2007-10-09 |
| CN1950490A (zh) | 2007-04-18 |
| GB0410134D0 (en) | 2004-06-09 |
| EP1743013A1 (en) | 2007-01-17 |
| EP1743013B1 (en) | 2007-12-19 |
| DE602005003937T2 (de) | 2008-12-18 |
| MXPA06012767A (es) | 2007-01-16 |
| US7687452B2 (en) | 2010-03-30 |
| WO2005108534A1 (en) | 2005-11-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0105 | International application |
Patent event date: 20061106 Patent event code: PA01051R01D Comment text: International Patent Application |
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| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |