KR0152173B1 - 시클로헥사놀유도체 이것을 함유하는 냉감제 및 냉감성조성물 및 이 유도체의 제조방법 및 그 중간체 - Google Patents
시클로헥사놀유도체 이것을 함유하는 냉감제 및 냉감성조성물 및 이 유도체의 제조방법 및 그 중간체 Download PDFInfo
- Publication number
- KR0152173B1 KR0152173B1 KR1019950701667A KR19957001667A KR0152173B1 KR 0152173 B1 KR0152173 B1 KR 0152173B1 KR 1019950701667 A KR1019950701667 A KR 1019950701667A KR 19957001667 A KR19957001667 A KR 19957001667A KR 0152173 B1 KR0152173 B1 KR 0152173B1
- Authority
- KR
- South Korea
- Prior art keywords
- compound
- general formula
- derivative
- cyclohexanol
- methylethyl
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 44
- HPXRVTGHNJAIIH-PTQBSOBMSA-N cyclohexanol Chemical class O[13CH]1CCCCC1 HPXRVTGHNJAIIH-PTQBSOBMSA-N 0.000 title claims abstract description 42
- 238000000034 method Methods 0.000 title description 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims description 66
- 239000003795 chemical substances by application Substances 0.000 claims description 15
- -1 benzyl halide Chemical class 0.000 claims description 14
- 239000002826 coolant Substances 0.000 claims description 13
- 238000004519 manufacturing process Methods 0.000 claims description 9
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 8
- 239000012312 sodium hydride Substances 0.000 claims description 8
- 229910000104 sodium hydride Inorganic materials 0.000 claims description 8
- IMCZVQCVSSWPCG-UHFFFAOYSA-N cyclohexyloxymethylbenzene Chemical class C=1C=CC=CC=1COC1CCCCC1 IMCZVQCVSSWPCG-UHFFFAOYSA-N 0.000 claims description 6
- 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 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229910052708 sodium Inorganic materials 0.000 claims description 4
- 239000011734 sodium Substances 0.000 claims description 4
- 229940100198 alkylating agent Drugs 0.000 claims description 3
- 239000002168 alkylating agent Substances 0.000 claims description 3
- 238000009903 catalytic hydrogenation reaction Methods 0.000 claims description 2
- 238000006460 hydrolysis reaction Methods 0.000 claims description 2
- 238000001816 cooling Methods 0.000 abstract description 23
- 210000002200 mouth mucosa Anatomy 0.000 abstract description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 32
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 31
- 238000006243 chemical reaction Methods 0.000 description 29
- 239000002904 solvent Substances 0.000 description 25
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 230000015572 biosynthetic process Effects 0.000 description 13
- 238000003786 synthesis reaction Methods 0.000 description 13
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- 239000007795 chemical reaction product Substances 0.000 description 11
- 230000000694 effects Effects 0.000 description 11
- 239000003814 drug Substances 0.000 description 10
- 239000012074 organic phase Substances 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000006071 cream Substances 0.000 description 9
- 239000007788 liquid Substances 0.000 description 9
- 238000004949 mass spectrometry Methods 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 8
- 239000002537 cosmetic Substances 0.000 description 8
- 239000006210 lotion Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 7
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 7
- 229940041616 menthol Drugs 0.000 description 7
- 239000006072 paste Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- 239000002585 base Substances 0.000 description 6
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 6
- 229940079593 drug Drugs 0.000 description 6
- 239000000543 intermediate Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000002453 shampoo Substances 0.000 description 6
- 239000012279 sodium borohydride Substances 0.000 description 6
- 229910000033 sodium borohydride Inorganic materials 0.000 description 6
- 235000015961 tonic Nutrition 0.000 description 6
- 230000001256 tonic effect Effects 0.000 description 6
- BINZTUGHCIRHLP-JOUUOIQHSA-N (1r,2s,5r)-2-(1-hydroxypropan-2-yl)-5-methylcyclohexan-1-ol Chemical compound OCC(C)[C@@H]1CC[C@@H](C)C[C@H]1O BINZTUGHCIRHLP-JOUUOIQHSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 150000002009 diols Chemical class 0.000 description 5
- 238000009472 formulation Methods 0.000 description 5
- ZYTMANIQRDEHIO-UHFFFAOYSA-N p-menth-8-en-3-ol Chemical compound CC1CCC(C(C)=C)C(O)C1 ZYTMANIQRDEHIO-UHFFFAOYSA-N 0.000 description 5
- 230000002688 persistence Effects 0.000 description 5
- 239000012071 phase Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000000606 toothpaste Substances 0.000 description 5
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- 235000016257 Mentha pulegium Nutrition 0.000 description 4
- 244000246386 Mentha pulegium Species 0.000 description 4
- 235000004357 Mentha x piperita Nutrition 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 239000006260 foam Substances 0.000 description 4
- 235000001050 hortel pimenta Nutrition 0.000 description 4
- 239000002674 ointment Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- RMNCXEZCLGGIIN-TVTJGUELSA-N (1r,2s,5r)-2-(1-methoxypropan-2-yl)-5-methylcyclohexan-1-ol Chemical compound COCC(C)[C@@H]1CC[C@@H](C)C[C@H]1O RMNCXEZCLGGIIN-TVTJGUELSA-N 0.000 description 3
- 229910015900 BF3 Inorganic materials 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000001525 mentha piperita l. herb oil Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- 235000019477 peppermint oil Nutrition 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 229940034610 toothpaste Drugs 0.000 description 3
- CAYDOSQIOPXLNA-SGUBAKSOSA-N (1r,2s,5r)-2-(1-ethoxypropan-2-yl)-5-methylcyclohexan-1-ol Chemical compound CCOCC(C)[C@@H]1CC[C@@H](C)C[C@H]1O CAYDOSQIOPXLNA-SGUBAKSOSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- RMNCXEZCLGGIIN-UHFFFAOYSA-N 2-(1-methoxypropan-2-yl)-5-methylcyclohexan-1-ol Chemical compound COCC(C)C1CCC(C)CC1O RMNCXEZCLGGIIN-UHFFFAOYSA-N 0.000 description 2
- AMKGKYQBASDDJB-UHFFFAOYSA-N 9$l^{2}-borabicyclo[3.3.1]nonane Chemical compound C1CCC2CCCC1[B]2 AMKGKYQBASDDJB-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 235000006679 Mentha X verticillata Nutrition 0.000 description 2
- 235000002899 Mentha suaveolens Nutrition 0.000 description 2
- 235000001636 Mentha x rotundifolia Nutrition 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 2
- KCXMKQUNVWSEMD-UHFFFAOYSA-N benzyl chloride Chemical compound ClCC1=CC=CC=C1 KCXMKQUNVWSEMD-UHFFFAOYSA-N 0.000 description 2
- 229940073608 benzyl chloride Drugs 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 235000009508 confectionery Nutrition 0.000 description 2
- DNTGGZPQPQTDQF-XBXARRHUSA-N crotamiton Chemical compound C/C=C/C(=O)N(CC)C1=CC=CC=C1C DNTGGZPQPQTDQF-XBXARRHUSA-N 0.000 description 2
- 229960003338 crotamiton Drugs 0.000 description 2
- 235000011850 desserts Nutrition 0.000 description 2
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 210000000245 forearm Anatomy 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 230000001771 impaired effect Effects 0.000 description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 230000035807 sensation Effects 0.000 description 2
- 235000019615 sensations Nutrition 0.000 description 2
- NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
- 235000014214 soft drink Nutrition 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 210000005182 tip of the tongue Anatomy 0.000 description 2
- 229960000716 tonics Drugs 0.000 description 2
- QATOZXKGBHJTKH-IBSWDFHHSA-N (1r,2s,5r)-5-methyl-2-(1-propan-2-yloxypropan-2-yl)cyclohexan-1-ol Chemical compound CC(C)OCC(C)[C@@H]1CC[C@@H](C)C[C@H]1O QATOZXKGBHJTKH-IBSWDFHHSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 229940090898 Desensitizer Drugs 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 244000062730 Melissa officinalis Species 0.000 description 1
- 235000010654 Melissa officinalis Nutrition 0.000 description 1
- 244000061176 Nicotiana tabacum Species 0.000 description 1
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000001347 alkyl bromides Chemical class 0.000 description 1
- 150000001348 alkyl chlorides Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000001351 alkyl iodides Chemical class 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- 238000005804 alkylation reaction Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
- 235000013361 beverage Nutrition 0.000 description 1
- 229910000085 borane Inorganic materials 0.000 description 1
- 229910010277 boron hydride Inorganic materials 0.000 description 1
- MCQRPQCQMGVWIQ-UHFFFAOYSA-N boron;methylsulfanylmethane Chemical compound [B].CSC MCQRPQCQMGVWIQ-UHFFFAOYSA-N 0.000 description 1
- UWTDFICHZKXYAC-UHFFFAOYSA-N boron;oxolane Chemical compound [B].C1CCOC1 UWTDFICHZKXYAC-UHFFFAOYSA-N 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000035601 cold sensitivity Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- DZGCGKFAPXFTNM-UHFFFAOYSA-N ethanol;hydron;chloride Chemical compound Cl.CCO DZGCGKFAPXFTNM-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 210000000887 face Anatomy 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000013355 food flavoring agent Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- HVTICUPFWKNHNG-UHFFFAOYSA-N iodoethane Chemical compound CCI HVTICUPFWKNHNG-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- FMKOJHQHASLBPH-UHFFFAOYSA-N isopropyl iodide Chemical compound CC(C)I FMKOJHQHASLBPH-UHFFFAOYSA-N 0.000 description 1
- 239000000865 liniment Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002324 mouth wash Substances 0.000 description 1
- 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 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 210000002850 nasal mucosa Anatomy 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- BZBAYMUKLAYQEO-UHFFFAOYSA-N phenylborane Chemical compound BC1=CC=CC=C1 BZBAYMUKLAYQEO-UHFFFAOYSA-N 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 238000007086 side reaction Methods 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/13—Saturated ethers containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/18—Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C43/188—Unsaturated ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/18—Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C43/196—Ethers having an ether-oxygen atom bound to a carbon atom of a ring other than a six-membered aromatic ring containing hydroxy or O-metal groups
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
- Fats And Perfumes (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP92-316438 | 1992-10-29 | ||
| JP31643892 | 1992-10-29 | ||
| PCT/JP1993/001562 WO1994010117A1 (fr) | 1992-10-29 | 1993-10-28 | Derive de cyclohexanol, agent et composition contenant ce derive destines a creer une sensation agreablement fraiche, procede pour produire ce derive, et intermediaire pour sa production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR0152173B1 true KR0152173B1 (ko) | 1998-10-15 |
Family
ID=18077091
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019950701667A Granted KR950704222A (ko) | 1992-10-29 | 1993-10-28 | 시클로헥사놀유도체 이것을 함유하는 냉감제 및 냉감성조성물 및 이 유도체의 제조방법 및 그 중간체(cyclohuxanol derivative, refrigerant and refrigerant composition containing the same, process for producing the derivative and intermediate therefor) |
| KR1019950701667A Expired - Lifetime KR0152173B1 (ko) | 1992-10-29 | 1993-10-28 | 시클로헥사놀유도체 이것을 함유하는 냉감제 및 냉감성조성물 및 이 유도체의 제조방법 및 그 중간체 |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019950701667A Granted KR950704222A (ko) | 1992-10-29 | 1993-10-28 | 시클로헥사놀유도체 이것을 함유하는 냉감제 및 냉감성조성물 및 이 유도체의 제조방법 및 그 중간체(cyclohuxanol derivative, refrigerant and refrigerant composition containing the same, process for producing the derivative and intermediate therefor) |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5756857A (enExample) |
| EP (1) | EP0667330B1 (enExample) |
| JP (1) | JP2770081B2 (enExample) |
| KR (2) | KR950704222A (enExample) |
| AU (1) | AU5344794A (enExample) |
| CA (1) | CA2147883C (enExample) |
| DE (1) | DE69312953T2 (enExample) |
| DK (1) | DK0667330T3 (enExample) |
| ES (1) | ES2105338T3 (enExample) |
| TW (1) | TW255884B (enExample) |
| WO (1) | WO1994010117A1 (enExample) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2978043B2 (ja) | 1993-09-16 | 1999-11-15 | 高砂香料工業株式会社 | （２ｓ）−３−｛（１ｒ，２ｓ，５ｒ）−［ ５−メチル−２−（１−メチルエチル）シクロヘキシル ］オキシ｝−１，２−プロパンジオール，その製造方法および用途 |
| DE69738913D1 (de) | 1997-09-18 | 2008-09-25 | Wrigley W M Jun Co | Kaugummi, enthaltend physiologisch kühlende wirkstoffe |
| US6455080B1 (en) | 1997-12-29 | 2002-09-24 | Wm. Wrigley Jr., Company | Chewing gum containing controlled release acyclic carboxamide and method of making |
| US6627233B1 (en) | 1997-09-18 | 2003-09-30 | Wm. Wrigley Jr. Company | Chewing gum containing physiological cooling agents |
| US6212663B1 (en) * | 1997-10-23 | 2001-04-03 | Sony Corporation | Apparatus and method for recovery of quantization codes in a lossy transmission environment |
| US6282684B1 (en) | 1997-10-23 | 2001-08-28 | Sony Corporation | Apparatus and method for recovery of data in a lossy transmission environment |
| US6307560B1 (en) | 1999-02-12 | 2001-10-23 | Sony Corporation | Classified adaptive spatio-temporal format conversion method and apparatus |
| US7010737B2 (en) * | 1999-02-12 | 2006-03-07 | Sony Corporation | Method and apparatus for error data recovery |
| US6519369B1 (en) | 1999-02-12 | 2003-02-11 | Sony Corporation | Method and apparatus for filter tap expansion |
| US6170074B1 (en) | 1999-02-12 | 2001-01-02 | Sony Corporation | Source coding to provide for robust error recovery |
| US6591398B1 (en) | 1999-02-12 | 2003-07-08 | Sony Corporation | Multiple processing system |
| US6389562B1 (en) | 1999-06-29 | 2002-05-14 | Sony Corporation | Source code shuffling to provide for robust error recovery |
| US6549672B1 (en) * | 1999-06-29 | 2003-04-15 | Sony Corporation | Method and apparatus for recovery of encoded data using central value |
| US6384263B1 (en) * | 2000-08-04 | 2002-05-07 | E. I. Du Pont De Nemours And Company | Process for making 3-hydroxyalkanelnitriles and conversion of the 3-hydroxyalkanelnitrile to an hydroxyaminoalkane |
| DE10058459A1 (de) * | 2000-11-24 | 2002-06-06 | Haarmann & Reimer Gmbh | Rhinologica |
| US20030229344A1 (en) * | 2002-01-22 | 2003-12-11 | Dycus Sean T. | Vessel sealer and divider and method of manufacturing same |
| US6972010B2 (en) * | 2001-04-17 | 2005-12-06 | The Procter & Gamble Company | Absorbent article comprising an agent able to convey a perception to the wearer, without the need to create the external condition perceived |
| US8273367B2 (en) * | 2001-04-17 | 2012-09-25 | The Procter And Gamble Company | Articles comprising a mint odor-free cooling agent |
| DE60334077D1 (de) * | 2003-05-19 | 2010-10-21 | Procter & Gamble | Flüchtiges Material enthaltender absobierender Hygieneartikel mit Sperrschichtverpackung |
| US8362264B2 (en) * | 2003-08-22 | 2013-01-29 | Dendreon Corporation | Compositions and methods for the treatment of disease associated with Trp-p8 expression |
| US7025997B2 (en) | 2003-09-24 | 2006-04-11 | International Flavors & Fragrances Inc. | Coolant plant extract compositions containing monomenthyl succinate |
| EP2559424A1 (en) | 2005-10-05 | 2013-02-20 | Kraft Foods Global Brands LLC | Cooling composition comprising trimethyl isopropyl butanamide |
| CA2634869C (en) | 2005-12-23 | 2012-03-06 | Cadbury Adams Usa Llc | Compositions providing a sensation substantially similar to that provided by menthol |
| US7772266B2 (en) | 2006-02-15 | 2010-08-10 | Dendreon Corporation | Small-molecule modulators of TRP-P8 activity |
| KR101457361B1 (ko) | 2006-02-15 | 2014-11-03 | 덴드레온 코포레이션 | Ｔｒｐｐ８ 활성 소-분자 조절자 |
| JP5371050B2 (ja) * | 2009-11-06 | 2013-12-18 | 住友精化株式会社 | ジボランの製造方法 |
| CN102792000B (zh) | 2010-04-27 | 2014-11-26 | 三菱重工业株式会社 | 二冲程发动机的扫气通路构造 |
| RU2014149076A (ru) | 2012-05-08 | 2016-06-27 | Мерк Патент Гмбх | Применение простых эфиров циклогексанола, обладающих антимикробными свойствами |
| DE102012016191A1 (de) | 2012-08-16 | 2014-03-13 | Merck Patent Gmbh | Verwendung von Cyclohexanolethern mit antimikrobiellen Eigenschaften |
| DE102012008892A1 (de) | 2012-05-08 | 2013-11-14 | Merck Patent Gmbh | Verwendung von Cyclohexanolethern mit antimikrobiellen Eigenschaften |
| KR102414963B1 (ko) | 2014-06-24 | 2022-07-01 | 코베스트로 도이칠란트 아게 | 니트로벤젠의 제조 방법 |
| FR3029777B1 (fr) | 2014-12-15 | 2019-11-29 | L'oreal | Utilisation de l'association d'un polyether polyurethane non-ionique associatif et d'un derive de cyclohexanol comme agent rafraichissant de la peau |
| MX2022010424A (es) * | 2020-03-05 | 2022-09-07 | Firmenich & Cie | Proceso de hidroboracion-oxidacion. |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2656385A (en) * | 1951-02-24 | 1953-10-20 | Upjohn Co | Cyclohexanols |
| GB1315625A (en) * | 1971-02-04 | 1973-05-02 | Wilkinson Sword Ltd | P-menthane diols and compositions containing them |
| BE795751A (fr) * | 1972-02-28 | 1973-08-21 | Unilever Nv | Compositions aromatisees contenant des composes qui donnent une sensation de froid |
| DE3440825A1 (de) * | 1984-11-08 | 1986-05-15 | Basf Ag, 6700 Ludwigshafen | P-alkoxy-cyclohexyl-alkanole und -alkanolester, deren herstellung und verwendung als riechstoffe |
| DE3705299A1 (de) * | 1987-02-19 | 1988-09-01 | Basf Ag | 3-tert-butyl-4-methoxi-cyclohexylmethanol, dessen herstellung und verwendung als riechstoff |
| US4757051A (en) * | 1987-08-11 | 1988-07-12 | Basf Aktiengesellschaft | 2-tert-butyl-4-methylcyclohexanol derivatives, their preparation and their use as scents |
| US5037802A (en) * | 1988-12-16 | 1991-08-06 | Basf K & F Corporation | Sandalwood odorants |
| JPH02290827A (ja) * | 1989-05-01 | 1990-11-30 | Kao Corp | １―アルコキシ―３―ｌ―メントキシプロパン―２―オール並びにこれを含有する冷感剤及び冷感性組成物 |
-
1993
- 1993-10-28 EP EP93923658A patent/EP0667330B1/en not_active Expired - Lifetime
- 1993-10-28 DK DK93923658.4T patent/DK0667330T3/da active
- 1993-10-28 CA CA002147883A patent/CA2147883C/en not_active Expired - Lifetime
- 1993-10-28 JP JP6510890A patent/JP2770081B2/ja not_active Expired - Lifetime
- 1993-10-28 KR KR1019950701667A patent/KR950704222A/ko active Granted
- 1993-10-28 KR KR1019950701667A patent/KR0152173B1/ko not_active Expired - Lifetime
- 1993-10-28 AU AU53447/94A patent/AU5344794A/en not_active Abandoned
- 1993-10-28 ES ES93923658T patent/ES2105338T3/es not_active Expired - Lifetime
- 1993-10-28 WO PCT/JP1993/001562 patent/WO1994010117A1/ja not_active Ceased
- 1993-10-28 US US08/433,375 patent/US5756857A/en not_active Expired - Lifetime
- 1993-10-28 DE DE69312953T patent/DE69312953T2/de not_active Expired - Lifetime
- 1993-11-15 TW TW082109522A patent/TW255884B/zh not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE69312953D1 (de) | 1997-09-11 |
| TW255884B (enExample) | 1995-09-01 |
| KR950704222A (ko) | 1995-11-17 |
| CA2147883A1 (en) | 1994-05-11 |
| JP2770081B2 (ja) | 1998-06-25 |
| US5756857A (en) | 1998-05-26 |
| EP0667330B1 (en) | 1997-08-06 |
| EP0667330A4 (enExample) | 1995-08-23 |
| ES2105338T3 (es) | 1997-10-16 |
| EP0667330A1 (en) | 1995-08-16 |
| DE69312953T2 (de) | 1998-03-05 |
| CA2147883C (en) | 2000-06-13 |
| WO1994010117A1 (fr) | 1994-05-11 |
| DK0667330T3 (da) | 1997-10-27 |
| AU5344794A (en) | 1994-05-24 |
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