CH512460A - Verfahren zur Herstellung von B-Jonon - Google Patents
Verfahren zur Herstellung von B-JononInfo
- Publication number
- CH512460A CH512460A CH56368A CH56368A CH512460A CH 512460 A CH512460 A CH 512460A CH 56368 A CH56368 A CH 56368A CH 56368 A CH56368 A CH 56368A CH 512460 A CH512460 A CH 512460A
- Authority
- CH
- Switzerland
- Prior art keywords
- ionone
- reaction
- pts
- water
- sulfuric acid
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title abstract 3
- 150000004657 carbamic acid derivatives Chemical class 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 13
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 53
- 238000006243 chemical reaction Methods 0.000 claims description 26
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 20
- 239000011541 reaction mixture Substances 0.000 claims description 19
- 229930195733 hydrocarbon Natural products 0.000 claims description 17
- 150000002430 hydrocarbons Chemical class 0.000 claims description 17
- 238000009835 boiling Methods 0.000 claims description 16
- 239000004215 Carbon black (E152) Substances 0.000 claims description 14
- 238000000034 method Methods 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 11
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 10
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 6
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 claims description 6
- 238000007363 ring formation reaction Methods 0.000 claims description 6
- 239000001282 iso-butane Substances 0.000 claims description 3
- 239000001294 propane Substances 0.000 claims description 3
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 238000010790 dilution Methods 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- 239000005457 ice water Substances 0.000 abstract description 7
- OWIKHYCFFJSOEH-UHFFFAOYSA-N Isocyanic acid Chemical compound N=C=O OWIKHYCFFJSOEH-UHFFFAOYSA-N 0.000 abstract 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-N anhydrous cyanic acid Natural products OC#N XLJMAIOERFSOGZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 238000011065 in-situ storage Methods 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 description 20
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 18
- 229930002839 ionone Natural products 0.000 description 10
- 150000002499 ionone derivatives Chemical class 0.000 description 10
- 239000003208 petroleum Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 8
- 239000010410 layer Substances 0.000 description 8
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 7
- HNZUNIKWNYHEJJ-UHFFFAOYSA-N geranyl acetone Natural products CC(C)=CCCC(C)=CCCC(C)=O HNZUNIKWNYHEJJ-UHFFFAOYSA-N 0.000 description 7
- JXJIQCXXJGRKRJ-KOOBJXAQSA-N pseudoionone Chemical compound CC(C)=CCC\C(C)=C\C=C\C(C)=O JXJIQCXXJGRKRJ-KOOBJXAQSA-N 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- 238000010626 work up procedure Methods 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000001273 butane Substances 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000012044 organic layer Substances 0.000 description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 description 4
- 239000002826 coolant Substances 0.000 description 3
- 230000036571 hydration Effects 0.000 description 3
- 238000006703 hydration reaction Methods 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000000376 reactant Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 230000001419 dependent effect Effects 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- UZFLPKAIBPNNCA-UHFFFAOYSA-N alpha-ionone Natural products CC(=O)C=CC1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-UHFFFAOYSA-N 0.000 description 1
- QWOXTGYXWFBKBF-UHFFFAOYSA-N butane;propan-2-one Chemical compound CCCC.CC(C)=O QWOXTGYXWFBKBF-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 235000011149 sulphuric acid Nutrition 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- UZFLPKAIBPNNCA-FPLPWBNLSA-N α-ionone Chemical compound CC(=O)\C=C/C1C(C)=CCCC1(C)C UZFLPKAIBPNNCA-FPLPWBNLSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/14—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms
- C07C403/16—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms not being part of —CHO 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
- C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL6700757A NL6700757A (en)) | 1967-01-18 | 1967-01-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH512460A true CH512460A (de) | 1971-09-15 |
Family
ID=19799018
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH56368A CH512460A (de) | 1967-01-18 | 1968-01-15 | Verfahren zur Herstellung von B-Jonon |
Country Status (7)
| Country | Link |
|---|---|
| AT (1) | AT281791B (en)) |
| BE (1) | BE709453A (en)) |
| CH (1) | CH512460A (en)) |
| DE (1) | DE1668505A1 (en)) |
| FR (1) | FR1550943A (en)) |
| GB (1) | GB1156443A (en)) |
| NL (1) | NL6700757A (en)) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3328440A1 (de) * | 1983-08-06 | 1985-02-21 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von jononen |
| DE3431131A1 (de) * | 1984-08-24 | 1986-03-06 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von jononen |
-
1967
- 1967-01-18 NL NL6700757A patent/NL6700757A/xx unknown
- 1967-12-02 DE DE19671668505 patent/DE1668505A1/de active Pending
-
1968
- 1968-01-15 AT AT38368A patent/AT281791B/de not_active IP Right Cessation
- 1968-01-15 CH CH56368A patent/CH512460A/de not_active IP Right Cessation
- 1968-01-16 FR FR1550943D patent/FR1550943A/fr not_active Expired
- 1968-01-16 GB GB2288/68A patent/GB1156443A/en not_active Expired
- 1968-01-16 BE BE709453D patent/BE709453A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE1668505A1 (de) | 1971-09-02 |
| BE709453A (en)) | 1968-07-16 |
| FR1550943A (en)) | 1968-12-20 |
| NL6700757A (en)) | 1968-07-19 |
| GB1156443A (en) | 1969-06-25 |
| AT281791B (de) | 1970-06-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2164767A1 (en)) | ||
| DE2547540A1 (de) | Verfahren zur herstellung von hydroxypivaldehyd | |
| CH643526A5 (de) | Verfahren zur herstellung von 2-hydroxynaphthalincarbonsaeuren. | |
| DE1493815B2 (de) | Verfahren zur gewinnung von reinem 2,2-(4,4' - dihydroxydiphenyl) - propan | |
| DE3237653A1 (de) | Verfahren zum synthetisieren von harnstoff | |
| DE2161215C3 (de) | Verfahren zur Herstellung von 5-Vinylnorbornen-(2) | |
| EP0133668B1 (de) | Verfahren zur Herstellung von Jononen | |
| CH512460A (de) | Verfahren zur Herstellung von B-Jonon | |
| DE1493977A1 (de) | Verfahren zur Herstellung von Hydrochinon aus p-Dialkylbenzol-bis-hydroperoxyden | |
| DE1917132C3 (de) | Verfahren zur Herstellung von ß -Jonon | |
| DE907171C (de) | Verfahren zur Abtrennung sauerstoffhaltiger Verbindungen aus Produkten der katalytrischen Kohlenoxydhydrierung | |
| DE2558399C3 (de) | Verfahren zur Herstellung von 3,6-Dichlorpicolinsäure | |
| DE3824518A1 (de) | Verfahren zur herstellung von 4,4-dimethyl-1-(p-chlor-phenyl)-pentan-3-on | |
| DE2435167B2 (de) | Verfahren zur Gewinnung von Guanidincarbonat aus verdünnten, wäßrigen Lösungen | |
| DE1017611B (de) | Verfahren zur Abtrennung von Begleitstoffen aus festen, kristallinen Stoffen oder Stoffgemischen | |
| DE2530859A1 (de) | Verfahren zum abtrennen von m- oder p-kresol | |
| DE2414597B2 (de) | Verfahren zur herstellung von alkalidithioniten | |
| DE933866C (de) | Verfahren zur Herstellung von Melamin aus Cyanamid | |
| DE2233489C3 (de) | Verfahren zur Herstellung von Octachlordipropyläther | |
| DE973281C (de) | Verfahren zur Chlorwasserstoffabspaltung aus Polychlorcyclohexanen | |
| DE951927C (de) | Verfahren zur Herstellung von meta-(Chlormethyl)-benzoesaeure | |
| DE820299C (de) | Verfahren zur Herstellung von Glutarsaeure | |
| CH645340A5 (de) | Verfahren zur herstellung von reinem, lagerbestaendigem acetoacetamid. | |
| DE2742978A1 (de) | Verfahren zur herstellung von cyanursaeure | |
| AT63818B (de) | Verfahren zur Darstellung von reinem Meta-Kresol. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |