JP2013519638A5 - - Google Patents
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- JP2013519638A5 JP2013519638A5 JP2012552358A JP2012552358A JP2013519638A5 JP 2013519638 A5 JP2013519638 A5 JP 2013519638A5 JP 2012552358 A JP2012552358 A JP 2012552358A JP 2012552358 A JP2012552358 A JP 2012552358A JP 2013519638 A5 JP2013519638 A5 JP 2013519638A5
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- 238000000034 method Methods 0.000 claims 17
- KHWTYGFHPHRQMP-UHFFFAOYSA-N (4-propan-2-ylcyclohexyl)methanol Chemical compound CC(C)C1CCC(CO)CC1 KHWTYGFHPHRQMP-UHFFFAOYSA-N 0.000 claims 5
- 239000003054 catalyst Substances 0.000 claims 5
- 229910052751 metal Inorganic materials 0.000 claims 5
- 239000002184 metal Substances 0.000 claims 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 4
- 150000001299 aldehydes Chemical class 0.000 claims 4
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 238000006198 methoxylation reaction Methods 0.000 claims 4
- 239000000203 mixture Substances 0.000 claims 4
- 230000000737 periodic effect Effects 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims 3
- 239000003792 electrolyte Substances 0.000 claims 3
- 238000005984 hydrogenation reaction Methods 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 229910000510 noble metal Inorganic materials 0.000 claims 3
- 229910052707 ruthenium Inorganic materials 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- WVDDGKGOMKODPV-UHFFFAOYSA-N hydroxymethyl benzene Natural products OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims 2
- -1 isopropylbenzyl alcohol Chemical compound 0.000 claims 2
- 239000000377 silicon dioxide Substances 0.000 claims 2
- 235000012239 silicon dioxide Nutrition 0.000 claims 2
- YEBHDRBQZQGMDS-UHFFFAOYSA-L tributyl(methyl)azanium;sulfate Chemical compound [O-]S([O-])(=O)=O.CCCC[N+](C)(CCCC)CCCC.CCCC[N+](C)(CCCC)CCCC YEBHDRBQZQGMDS-UHFFFAOYSA-L 0.000 claims 2
- ZETHHMPKDUSZQQ-UHFFFAOYSA-N Betulafolienepentol Natural products C1C=C(C)CCC(C(C)CCC=C(C)C)C2C(OC)OC(OC)C2=C1 ZETHHMPKDUSZQQ-UHFFFAOYSA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- PCSMJKASWLYICJ-UHFFFAOYSA-N Succinic aldehyde Chemical compound O=CCCC=O PCSMJKASWLYICJ-UHFFFAOYSA-N 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 235000019445 benzyl alcohol Nutrition 0.000 claims 1
- HEOKFDGOFROELJ-UHFFFAOYSA-N diacetal Natural products COc1ccc(C=C/c2cc(O)cc(OC3OC(COC(=O)c4cc(O)c(O)c(O)c4)C(O)C(O)C3O)c2)cc1O HEOKFDGOFROELJ-UHFFFAOYSA-N 0.000 claims 1
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 claims 1
- 239000007789 gas Substances 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 230000003301 hydrolyzing effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 230000035515 penetration Effects 0.000 claims 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims 1
- 229910052703 rhodium Inorganic materials 0.000 claims 1
- 239000010948 rhodium Substances 0.000 claims 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims 1
- 230000007704 transition Effects 0.000 claims 1
- DELBDSAYZQPUSX-UHFFFAOYSA-L triethyl(methyl)azanium;sulfate Chemical compound [O-]S([O-])(=O)=O.CC[N+](C)(CC)CC.CC[N+](C)(CC)CC DELBDSAYZQPUSX-UHFFFAOYSA-L 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10153392.5 | 2010-02-12 | ||
| EP10153392 | 2010-02-12 | ||
| PCT/EP2011/051770 WO2011098432A2 (de) | 2010-02-12 | 2011-02-08 | Verfahren zur herstellung von 4-isopropylcyclohexylmethanol |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013519638A JP2013519638A (ja) | 2013-05-30 |
| JP2013519638A5 true JP2013519638A5 (enExample) | 2014-04-03 |
Family
ID=43927841
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012552358A Pending JP2013519638A (ja) | 2010-02-12 | 2011-02-08 | ４−イソプロピルシクロヘキシルメタノールの製造方法 |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP2534281B1 (enExample) |
| JP (1) | JP2013519638A (enExample) |
| CN (1) | CN102762774A (enExample) |
| ES (1) | ES2719585T3 (enExample) |
| MX (1) | MX345325B (enExample) |
| WO (1) | WO2011098432A2 (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015527483A (ja) * | 2012-06-15 | 2015-09-17 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | 求核試薬の存在下での有機基材の陽極酸化 |
| EP4230612B1 (en) * | 2020-10-19 | 2025-12-03 | Mitsubishi Gas Chemical Company, Inc. | Alicyclic alcohol, alicyclic alcohol composition, and perfume composition |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH578312A5 (enExample) | 1973-06-07 | 1976-08-13 | Firmenich & Cie | |
| DE3322399A1 (de) * | 1983-06-22 | 1985-01-10 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von benz aldehyddialkylacetalen |
| DE3644076A1 (de) * | 1986-12-23 | 1988-07-07 | Basf Ag | Neue benzaldehydderivate, ihre herstellung und verwendung |
| DE3718564A1 (de) * | 1987-06-03 | 1988-12-15 | Basf Ag | Verfahren zur herstellung von 4-isopropyl-cyclohexylmethanol bzw. dessen alkylethern |
| ES2009174A6 (es) * | 1988-02-09 | 1989-09-01 | Barba Merino Isidoro | Obtencion de cuminal y cuminal dimetil acetal por metoxilacion anodica de p-cimeno. |
| DE4201544A1 (de) * | 1992-01-22 | 1993-07-29 | Basf Ag | Verfahren zur herstellung von benzaldehydacetalen |
| DE4308846A1 (de) * | 1993-03-19 | 1994-09-22 | Basf Ag | Verfahren zur Herstellung von Terephthalaldehydtetraalkylacetalen |
| DE4327361A1 (de) | 1993-08-14 | 1995-02-16 | Basf Ag | Verfahren zur Herstellung von Benzaldehyddialkylacetalen |
| US6248924B1 (en) * | 1996-06-19 | 2001-06-19 | Basf Aktiengesellschaft | Process for reacting an organic compound in the presence of a supported ruthenium catalyst |
| DE19904900A1 (de) | 1998-06-26 | 1999-12-30 | Basf Ag | Verfahren zur Herstellung von Alkoxymethylaromaten |
| DE19844325A1 (de) * | 1998-09-28 | 2000-03-30 | Degussa | Verfahren zur Herstellung von Alkoholen durch katalytische Hydrierung von Aldehyden oder Ketonen |
| DE10058304A1 (de) * | 2000-11-24 | 2002-05-29 | Basf Ag | Verfahren zur Herstellung von alkoxylierten Carbonylverbindungen durch ein anodisches Oxidationsverfahren unter Nutzung der kathodischen Koppelreaktion zur organischen Synthese |
| DE10063195A1 (de) * | 2000-12-19 | 2002-06-20 | Basf Ag | Bipolare quasigeteilte Elektrolysezellen |
| KR100710559B1 (ko) * | 2003-02-12 | 2007-04-24 | 에스케이 주식회사 | 고효율의 1-시클로헥실-1-에탄올의 제조방법 |
| DE102004011427A1 (de) | 2004-03-09 | 2005-09-29 | Basf Ag | Absorptionsmittel mit verbesserter Oxidationsbeständigkeit und Verfahren zum Entsäuern von Fluidströmen |
| DE102005029200A1 (de) | 2005-06-22 | 2006-12-28 | Basf Ag | Katalysator und Verfahren zur Hydrierung von hydrierbare Gruppen enthaltenden organischen Verbindungen |
| WO2009059944A1 (de) | 2007-11-06 | 2009-05-14 | Basf Se | Elektrochemisches verfahren zur herstellung von benzaldehyddimethylacetalen |
| WO2009059941A1 (de) | 2007-11-06 | 2009-05-14 | Basf Se | Verfahren zur regioselektiven alkoxyalkylierung von substituierten benzolen |
| WO2010079035A2 (de) | 2008-12-17 | 2010-07-15 | Basf Se | Kontinuierliches verfahren zur herstellung von substituierten cyclohexylmethanolen |
-
2011
- 2011-02-08 JP JP2012552358A patent/JP2013519638A/ja active Pending
- 2011-02-08 ES ES11704430T patent/ES2719585T3/es active Active
- 2011-02-08 CN CN2011800093602A patent/CN102762774A/zh active Pending
- 2011-02-08 MX MX2012009124A patent/MX345325B/es active IP Right Grant
- 2011-02-08 EP EP11704430.5A patent/EP2534281B1/de active Active
- 2011-02-08 WO PCT/EP2011/051770 patent/WO2011098432A2/de not_active Ceased
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