DE2810107C2 - 13-Oxabicyclo[10.3.0]pentadecan, Verfahren zu dessen Herstellung und dessen Verwendung als Riechstoff - Google Patents
13-Oxabicyclo[10.3.0]pentadecan, Verfahren zu dessen Herstellung und dessen Verwendung als RiechstoffInfo
- Publication number
- DE2810107C2 DE2810107C2 DE2810107A DE2810107A DE2810107C2 DE 2810107 C2 DE2810107 C2 DE 2810107C2 DE 2810107 A DE2810107 A DE 2810107A DE 2810107 A DE2810107 A DE 2810107A DE 2810107 C2 DE2810107 C2 DE 2810107C2
- Authority
- DE
- Germany
- Prior art keywords
- pentadecane
- oxabicyclo
- weight
- parts
- preparation
- 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
Links
- BXUHYORBIXEKMH-UHFFFAOYSA-N 2,3,3a,4,5,6,7,8,9,10,11,12,13,13a-tetradecahydrocyclododeca[b]furan Chemical compound C1CCCCCCCCCC2OCCC21 BXUHYORBIXEKMH-UHFFFAOYSA-N 0.000 title claims description 14
- 239000003205 fragrance Substances 0.000 title claims description 7
- 238000002360 preparation method Methods 0.000 title claims description 6
- 238000000034 method Methods 0.000 title claims description 3
- 150000002596 lactones Chemical class 0.000 claims description 7
- 150000002009 diols Chemical class 0.000 claims description 6
- -1 hydroxy ester Chemical class 0.000 claims description 5
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 3
- 239000012279 sodium borohydride Substances 0.000 claims description 3
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000000203 mixture Substances 0.000 description 16
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- SXVPOSFURRDKBO-UHFFFAOYSA-N Cyclododecanone Chemical compound O=C1CCCCCCCCCCC1 SXVPOSFURRDKBO-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 230000007935 neutral effect Effects 0.000 description 4
- 239000002304 perfume Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- FKUPPRZPSYCDRS-UHFFFAOYSA-N Cyclopentadecanolide Chemical compound O=C1CCCCCCCCCCCCCCO1 FKUPPRZPSYCDRS-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 101100311330 Schizosaccharomyces pombe (strain 972 / ATCC 24843) uap56 gene Proteins 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- ISAOCJYIOMOJEB-UHFFFAOYSA-N benzoin Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 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
- 238000001035 drying Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- HPTIDIPGIUCQFC-UHFFFAOYSA-N methoxymethoxycyclododecane Chemical compound COCOC1CCCCCCCCCCC1 HPTIDIPGIUCQFC-UHFFFAOYSA-N 0.000 description 2
- 101150018444 sub2 gene Proteins 0.000 description 2
- 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
- MJBLBGCUTIKTJT-UHFFFAOYSA-N 1-(5,5-dimethyl-4-propan-2-yl-1,3-dioxan-2-yl)ethanone Chemical compound CC(C)C1OC(C(C)=O)OCC1(C)C MJBLBGCUTIKTJT-UHFFFAOYSA-N 0.000 description 1
- NFAVNWJJYQAGNB-UHFFFAOYSA-N 2-methylundecanal Chemical compound CCCCCCCCCC(C)C=O NFAVNWJJYQAGNB-UHFFFAOYSA-N 0.000 description 1
- WXCMHFPAUCOJIG-UHFFFAOYSA-N 4'-tert-Butyl-2',6'-dimethyl-3',5'-dinitroacetophenone Chemical compound CC(=O)C1=C(C)C([N+]([O-])=O)=C(C(C)(C)C)C([N+]([O-])=O)=C1C WXCMHFPAUCOJIG-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 244000223760 Cinnamomum zeylanicum Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 244000028419 Styrax benzoin Species 0.000 description 1
- 235000000126 Styrax benzoin Nutrition 0.000 description 1
- 235000008411 Sumatra benzointree Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 229960002130 benzoin Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- DJYWGTBEZVORGE-CVWWDKSYSA-N cedr-8(15)-en-9-ol Chemical compound C1[C@]23[C@H](C)CC[C@H]3C(C)(C)[C@@H]1C(=C)C(O)C2 DJYWGTBEZVORGE-CVWWDKSYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000017803 cinnamon Nutrition 0.000 description 1
- 239000010633 clary sage oil Substances 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000002979 fabric softener Substances 0.000 description 1
- 235000019382 gum benzoic Nutrition 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- LVECZGHBXXYWBO-UHFFFAOYSA-N pentadecanolide Natural products CC1CCCCCCCCCCCCC(=O)O1 LVECZGHBXXYWBO-UHFFFAOYSA-N 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000001738 pogostemon cablin oil Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
- C11B9/00—Essential oils; Perfumes
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
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)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
- Furan Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2810107A DE2810107C2 (de) | 1978-03-09 | 1978-03-09 | 13-Oxabicyclo[10.3.0]pentadecan, Verfahren zu dessen Herstellung und dessen Verwendung als Riechstoff |
| US06/016,548 US4222904A (en) | 1978-03-09 | 1979-03-01 | 13-Oxabicyclo[10.3.0]pentadecane, its preparation and use in perfume compositions and as an odorant |
| IT20712/79A IT1113429B (it) | 1978-03-09 | 1979-03-02 | 13-oxabiciclo aperta par.quadra 10.3.0 chiusa par.quadra pentadecano,come profumo,sua produzione e composizioni di profumi che lo contengono |
| EP79100645A EP0004052B1 (de) | 1978-03-09 | 1979-03-05 | 13-Oxabicyclo(10.3.0)pentadecan, dessen Herstellung und Verwendung als Riechstoff, sowie dieses enthaltende Riechstoffkompositionen |
| MX176823A MX150170A (es) | 1978-03-09 | 1979-03-06 | El nuevo uso de caracter industrial del 13-oxabiciclo(10.3.0)pentadecano para impartir aroma de ambar en perfumeria |
| JP2622679A JPS54122266A (en) | 1978-03-09 | 1979-03-08 | 133oxabicyclo*10*3*0*pentadecane*its manufacture and perfume containing it or made from it |
| ES478433A ES478433A1 (es) | 1978-03-09 | 1979-03-08 | Procedimiento para la obtencion de 13-oxabiciclo 10,3,0-pen-tadecano. |
| BR7901398A BR7901398A (pt) | 1978-03-09 | 1979-03-08 | Composto,processo para sua producao,sua aplicacao,e composicoes de materiais de perfume |
| CA323,045A CA1093568A (en) | 1978-03-09 | 1979-03-09 | 13-oxabicyclo ¬10.3.0| pentadecane, its preparation and use in perfume compositions and as an odorant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2810107A DE2810107C2 (de) | 1978-03-09 | 1978-03-09 | 13-Oxabicyclo[10.3.0]pentadecan, Verfahren zu dessen Herstellung und dessen Verwendung als Riechstoff |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2810107A1 DE2810107A1 (de) | 1979-09-13 |
| DE2810107C2 true DE2810107C2 (de) | 1987-01-22 |
Family
ID=6033909
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2810107A Expired DE2810107C2 (de) | 1978-03-09 | 1978-03-09 | 13-Oxabicyclo[10.3.0]pentadecan, Verfahren zu dessen Herstellung und dessen Verwendung als Riechstoff |
Country Status (9)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3040994A1 (de) * | 1980-10-31 | 1982-06-09 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur herstellung von 13-oxabicyclo 10.3.0 -pentadecan |
| DE3137939A1 (de) * | 1981-09-24 | 1983-05-19 | Consortium für elektrochemische Industrie GmbH, 8000 München | "substituierte macrobicyclische ether, deren herstellung und verwendung" |
| DE3400690A1 (de) * | 1984-01-11 | 1985-07-18 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von 13-oxabicyclo(10.3.0)-pentadecan |
| US6346510B1 (en) | 1995-10-23 | 2002-02-12 | The Children's Medical Center Corporation | Therapeutic antiangiogenic endostatin compositions |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3085107A (en) * | 1960-11-28 | 1963-04-09 | Rhone Poulenc Sa | Cyclododecylacetic acid esters, derivatives thereof and intermediates therefor |
| BE786518A (fr) * | 1971-07-21 | 1973-01-22 | Haarmann & Reimer Gmbh | Procede de preparation d'oxa-bicyclo-alcenes |
| DE2209372C2 (de) * | 1972-02-28 | 1973-09-27 | Dragoco Spezialfarik Konzentrierter Riech- Und Aromastoffe Gerberding & Co Gmbh, 3450 Holzminden | 3 Oxa bicyclo eckige Klammer auf 10 3 0 eckige Klammer zu pentadecen (6) und ein Verfahren zu dessen Her stellung sowie dessen Verwendung als Riechstoff |
-
1978
- 1978-03-09 DE DE2810107A patent/DE2810107C2/de not_active Expired
-
1979
- 1979-03-01 US US06/016,548 patent/US4222904A/en not_active Expired - Lifetime
- 1979-03-02 IT IT20712/79A patent/IT1113429B/it active
- 1979-03-05 EP EP79100645A patent/EP0004052B1/de not_active Expired
- 1979-03-06 MX MX176823A patent/MX150170A/es unknown
- 1979-03-08 BR BR7901398A patent/BR7901398A/pt unknown
- 1979-03-08 ES ES478433A patent/ES478433A1/es not_active Expired
- 1979-03-08 JP JP2622679A patent/JPS54122266A/ja active Granted
- 1979-03-09 CA CA323,045A patent/CA1093568A/en not_active Expired
Non-Patent Citations (1)
| Title |
|---|
| NICHTS-ERMITTELT |
Also Published As
| Publication number | Publication date |
|---|---|
| IT7920712A0 (it) | 1979-03-02 |
| US4222904A (en) | 1980-09-16 |
| CA1093568A (en) | 1981-01-13 |
| IT1113429B (it) | 1986-01-20 |
| BR7901398A (pt) | 1979-10-02 |
| EP0004052B1 (de) | 1982-10-06 |
| DE2810107A1 (de) | 1979-09-13 |
| MX150170A (es) | 1984-03-29 |
| ES478433A1 (es) | 1979-05-16 |
| EP0004052A1 (de) | 1979-09-19 |
| JPS54122266A (en) | 1979-09-21 |
| JPS62912B2 (US20030157025A1-20030821-C00031.png) | 1987-01-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2626142A1 (de) | Verwendung von aliphatischen 2-methyl- 2-alkyl-alkansaeureestern als riechstoffe sowie diese enthaltende riechstoffkompositionen | |
| EP0857723A1 (de) | Cyclische Cedren-Acetale, ihre Herstellung und ihre Verwendung | |
| EP0033928A2 (de) | Verwendung alkylsubstituierter 1,3-Dioxolane als Riechstoffe, sowie diese enthaltende Riechstoffkompositionen | |
| DE2910579C2 (US20030157025A1-20030821-C00031.png) | ||
| DE2810107C2 (de) | 13-Oxabicyclo[10.3.0]pentadecan, Verfahren zu dessen Herstellung und dessen Verwendung als Riechstoff | |
| EP0023612B1 (de) | Makrocyclische Diester, Verfahren zu ihrer Herstellung und ihre Verwendung als Riechstoffe | |
| EP0301375A2 (de) | Bicyclische Aldehyde | |
| EP0021356A1 (de) | 4(5)-Acetyl-7,7,9(7,9,9)-trimethyl-bicyclo(4.3.0)-non-1-en, dessen Herstellung und Verwendung als Riechstoff, sowie dieses enthaltende Riechstoffkompositionen | |
| EP0043507B1 (de) | 2,4-Dioxa-7,10-methano-spiro(5,5)undecane, deren Herstellung sowie diese enthaltende Riechstoffkompositionen | |
| EP0025869B1 (de) | 3-Methyl-cyclohexadecen-5-on-1, Verfahren zu seiner Herstellung und seine Verwendung als Riechstoff | |
| EP0006572B1 (de) | 13,15-Dioxabicyclo (10.5.0) heptadecane, deren Herstellung und Verwendung als Riechstoff sowie diese enthaltende Riechstoffkompositionen | |
| EP0395982B1 (de) | Beta,gamma-Ungesättigte Nitrile, deren Herstellung und Verwendung als Riechstoffe | |
| DE3639158A1 (de) | 1-methyl-3-(p-methyl-phenyl)-propionitril, dessen herstellung und verwendung als riechstoff | |
| DE2517620A1 (de) | Verwendung von exo-norbornyl-2- essigsaeureestern als riechstoffe sowie diese enthaltende riechstoffkompositionen | |
| DE2945812A1 (de) | 1,5-dimethyl-bicyclo eckige klammer auf 3,2,1 eckige klammer zu octan-derivate, verfahren zu ihrer herstellung und ihre verwendung | |
| EP0093853A1 (de) | Substituierte 3-Isopropyl-cyclopentanonderivate, deren Herstellung und Verwendung als Riechstoffe sowie diese enthaltende Riechstoffkompositionen | |
| EP0025182B1 (de) | 3-Methyl-1,4-dioxa-bicyclo(4.4.0)decan-2-on, dessen Herstellung und Verwendung als Riechstoff sowie dieses enthaltende Riechstoffkompositionen | |
| EP0340645B1 (de) | Isomere Formyl-trimethylbicyclo(2,2,2)oct-7-ene | |
| DE2934678A1 (de) | Cyclopentadecen-8-on-1, verfahren zu seiner herstellung und seine verwendung als riechstoff | |
| EP0053717B1 (de) | Terpenderivate, deren Herstellung, Verwendung als Riechstoffe sowie diese enthaltende Riechstoffkompositionen | |
| EP0085937B1 (de) | Riechstoff mit tricyclischer Ringstruktur | |
| EP0120290B1 (de) | Oxaspirododecan-Derivate, deren Herstellung und Verwendung als Riechstoffe sowie diese enthaltende Riechstoffkompositionen | |
| EP0586442B1 (de) | Verwendung isomerer 1,1,1-trialkyl-2-phenyl-ethan-derivate als riechstoffe, sowie diese enthaltende riechstoffkompositionen | |
| EP0330995B1 (de) | Bicyclische Aether | |
| EP0211303A2 (de) | 2-Acyl-5-methylfurane, ein Verfahren zu ihrer Herstellung und ihre Verwendung |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8110 | Request for examination paragraph 44 | ||
| 8181 | Inventor (new situation) |
Free format text: MEINS, PETER, DIPL.-CHEM. DR., 4020 METTMANN, DE BRUNS, KLAUS, DIPL.-CHEM. DR., 4150 KREFELD, DE |
|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |