JPS6215552B2 - - Google Patents
Info
- Publication number
- JPS6215552B2 JPS6215552B2 JP53091661A JP9166178A JPS6215552B2 JP S6215552 B2 JPS6215552 B2 JP S6215552B2 JP 53091661 A JP53091661 A JP 53091661A JP 9166178 A JP9166178 A JP 9166178A JP S6215552 B2 JPS6215552 B2 JP S6215552B2
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- trimethyl
- dioxane
- weight
- acid
- 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
- GAGMMTUVMITPBL-UHFFFAOYSA-N 2,2,5-trimethyl-5-phenyl-1,3-dioxane Chemical compound C1OC(C)(C)OCC1(C)C1=CC=CC=C1 GAGMMTUVMITPBL-UHFFFAOYSA-N 0.000 claims description 4
- 239000003205 fragrance Substances 0.000 claims description 4
- HEWZVZIVELJPQZ-UHFFFAOYSA-N 2,2-dimethoxypropane Chemical compound COC(C)(C)OC HEWZVZIVELJPQZ-UHFFFAOYSA-N 0.000 claims description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 3
- 239000003054 catalyst Substances 0.000 claims description 2
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical compound C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 claims 2
- WKONZEGQQJMKKC-UHFFFAOYSA-N CC1OC(C)(C)OCC1C1=CC=CC=C1 Chemical compound CC1OC(C)(C)OCC1C1=CC=CC=C1 WKONZEGQQJMKKC-UHFFFAOYSA-N 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000002304 perfume Substances 0.000 description 13
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- OOCCDEMITAIZTP-QPJJXVBHSA-N (E)-cinnamyl alcohol Chemical compound OC\C=C\C1=CC=CC=C1 OOCCDEMITAIZTP-QPJJXVBHSA-N 0.000 description 2
- FLUWAIIVLCVEKF-UHFFFAOYSA-N 2-Methyl-1-phenyl-2-propanyl acetate Chemical compound CC(=O)OC(C)(C)CC1=CC=CC=C1 FLUWAIIVLCVEKF-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229940095104 dimethyl benzyl carbinyl acetate Drugs 0.000 description 2
- CBOQJANXLMLOSS-UHFFFAOYSA-N ethyl vanillin Chemical compound CCOC1=CC(C=O)=CC=C1O CBOQJANXLMLOSS-UHFFFAOYSA-N 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 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
- RIWRBSMFKVOJMN-UHFFFAOYSA-N 2-methyl-1-phenylpropan-2-ol Chemical compound CC(C)(O)CC1=CC=CC=C1 RIWRBSMFKVOJMN-UHFFFAOYSA-N 0.000 description 1
- UCAGGGXNNMODQS-UHFFFAOYSA-N 2-methyl-2-phenylpropane-1,1-diol Chemical compound OC(O)C(C)(C)C1=CC=CC=C1 UCAGGGXNNMODQS-UHFFFAOYSA-N 0.000 description 1
- KVKKTLBBYFABAZ-UHFFFAOYSA-N 2-phenylethyl 2-methylbutanoate Chemical compound CCC(C)C(=O)OCCC1=CC=CC=C1 KVKKTLBBYFABAZ-UHFFFAOYSA-N 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- 240000007466 Lilium auratum Species 0.000 description 1
- 235000002159 Lilium auratum Nutrition 0.000 description 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 1
- 241000220317 Rosa Species 0.000 description 1
- 238000007171 acid catalysis Methods 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- OOCCDEMITAIZTP-UHFFFAOYSA-N allylic benzylic alcohol Natural products OCC=CC1=CC=CC=C1 OOCCDEMITAIZTP-UHFFFAOYSA-N 0.000 description 1
- 235000019568 aromas Nutrition 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000010632 citronella oil Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 229940019836 cyclamen aldehyde Drugs 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229940073505 ethyl vanillin Drugs 0.000 description 1
- -1 gargles Substances 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WPFVBOQKRVRMJB-UHFFFAOYSA-N hydroxycitronellal Chemical compound O=CCC(C)CCCC(C)(C)O WPFVBOQKRVRMJB-UHFFFAOYSA-N 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- 230000005923 long-lasting effect Effects 0.000 description 1
- JPTOCTSNXXKSSN-UHFFFAOYSA-N methylheptenone Chemical compound CCCC=CC(=O)CC JPTOCTSNXXKSSN-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- SATCULPHIDQDRE-UHFFFAOYSA-N piperonal Chemical compound O=CC1=CC=C2OCOC2=C1 SATCULPHIDQDRE-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- ZFNVDHOSLNRHNN-UHFFFAOYSA-N xi-3-(4-Isopropylphenyl)-2-methylpropanal Chemical compound O=CC(C)CC1=CC=C(C(C)C)C=C1 ZFNVDHOSLNRHNN-UHFFFAOYSA-N 0.000 description 1
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
- C11B9/0069—Heterocyclic compounds
- C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
- C11B9/008—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing six atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D319/04—1,3-Dioxanes; Hydrogenated 1,3-dioxanes
- C07D319/06—1,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
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)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19772734295 DE2734295A1 (de) | 1977-07-29 | 1977-07-29 | 2,2,5-trimethyl-5-phenyl-1,3-dioxan, dessen herstellung, verwendung als riechstoff, sowie dieses enthaltende riechstoffkompositionen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5427576A JPS5427576A (en) | 1979-03-01 |
| JPS6215552B2 true JPS6215552B2 (US07122547-20061017-C00032.png) | 1987-04-08 |
Family
ID=6015177
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP9166178A Granted JPS5427576A (en) | 1977-07-29 | 1978-07-28 | 2*2*55trimethyll55phenyll 1*33doxane * production thereof and ferfume containing same |
Country Status (6)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0017397A1 (en) * | 1979-04-06 | 1980-10-15 | TATE & LYLE PATENT HOLDINGS LIMITED | Sugar acetals, their preparation and use |
| NL8005518A (nl) | 1980-10-06 | 1982-05-03 | Naarden & Shell Aroma Chem | Parfumcomposities en geparfumeerde materialen en voorwerpen, die fenyl-tetrahydrofuranen als reukstof bevatten. |
| US4549029A (en) * | 1983-04-05 | 1985-10-22 | Givaudan Corporation | Substituted tetrahydrofurans |
| JPS6095467U (ja) * | 1983-11-30 | 1985-06-29 | 東洋ラジエーター株式会社 | 積層型熱交換器 |
| DE19822232A1 (de) * | 1998-05-07 | 1999-11-11 | Dragoco Gerberding Co Ag | 2,4,6-Trimethyl-4-phenyl-1,3-dioxan |
| DE10022417A1 (de) * | 2000-05-09 | 2001-11-15 | Cognis Deutschland Gmbh | Cyclische Ketale |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2993055A (en) * | 1958-10-02 | 1961-07-18 | Dow Chemical Co | 8-tert-butyl-1, 4-dioxaspiro[4.5]-decane |
| US3239421A (en) * | 1964-09-29 | 1966-03-08 | United States Borax Chem | Perfume composition containing 2-(betaphenylethoxy)-4, 4, 6-trimethyl-1, 3-dioxa-2-borinane |
| NL166187C (nl) * | 1973-04-18 | 1981-07-15 | Naarden International Nv | Werkwijze ter bereiding van reukstofcomposities door een 2-gesubstitueerd 4,4,6-trimethyl-1,3-dioxan te mengen met ten minste een andere reukstof en geparfu- meerde voorwerpen. |
| DE2604553C2 (de) * | 1976-02-06 | 1985-01-24 | Henkel KGaA, 4000 Düsseldorf | 2,4-Dioxa-spiro(5,5)undec-8-ene und diese Verbindungen enthaltende Riechstoffkompositionen |
-
1977
- 1977-07-29 DE DE19772734295 patent/DE2734295A1/de not_active Withdrawn
-
1978
- 1978-05-15 GB GB19476/78A patent/GB1601859A/en not_active Expired
- 1978-07-07 NL NL7807381A patent/NL7807381A/xx not_active Application Discontinuation
- 1978-07-12 US US05/923,794 patent/US4198323A/en not_active Expired - Lifetime
- 1978-07-28 JP JP9166178A patent/JPS5427576A/ja active Granted
- 1978-07-28 FR FR7822478A patent/FR2398743A1/fr active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| GB1601859A (en) | 1981-11-04 |
| JPS5427576A (en) | 1979-03-01 |
| FR2398743B1 (US07122547-20061017-C00032.png) | 1981-07-17 |
| NL7807381A (nl) | 1979-01-31 |
| US4198323A (en) | 1980-04-15 |
| DE2734295A1 (de) | 1979-02-08 |
| FR2398743A1 (fr) | 1979-02-23 |
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