DE1793209A1 - Verzweigtkettige,aliphatische Ester und Verfahren zu ihrer Herstellung - Google Patents
Verzweigtkettige,aliphatische Ester und Verfahren zu ihrer HerstellungInfo
- Publication number
- DE1793209A1 DE1793209A1 DE19681793209 DE1793209A DE1793209A1 DE 1793209 A1 DE1793209 A1 DE 1793209A1 DE 19681793209 DE19681793209 DE 19681793209 DE 1793209 A DE1793209 A DE 1793209A DE 1793209 A1 DE1793209 A1 DE 1793209A1
- Authority
- DE
- Germany
- Prior art keywords
- hydrocarbon
- carbene
- esters
- ethyl
- carbon atoms
- 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.)
- Pending
Links
- 238000000034 method Methods 0.000 title claims description 12
- 125000001931 aliphatic group Chemical group 0.000 title description 4
- 238000002360 preparation method Methods 0.000 title description 3
- 150000002148 esters Chemical class 0.000 claims description 30
- 150000002430 hydrocarbons Chemical class 0.000 claims description 25
- 239000004215 Carbon black (E152) Substances 0.000 claims description 24
- 229930195733 hydrocarbon Natural products 0.000 claims description 24
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 21
- 239000002243 precursor Substances 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 238000000354 decomposition reaction Methods 0.000 claims description 5
- 150000008049 diazo compounds Chemical class 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims 1
- 150000004845 diazirines Chemical class 0.000 claims 1
- 239000000446 fuel Substances 0.000 claims 1
- 238000011065 in-situ storage Methods 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 239000000376 reactant Substances 0.000 claims 1
- DCAYPVUWAIABOU-UHFFFAOYSA-N hexadecane Chemical compound CCCCCCCCCCCCCCCC DCAYPVUWAIABOU-UHFFFAOYSA-N 0.000 description 20
- -1 tetradeoan Chemical compound 0.000 description 13
- 239000000203 mixture Substances 0.000 description 10
- 150000001735 carboxylic acids Chemical class 0.000 description 8
- 238000006243 chemical reaction Methods 0.000 description 8
- HOWGUJZVBDQJKV-UHFFFAOYSA-N docosane Chemical compound CCCCCCCCCCCCCCCCCCCCCC HOWGUJZVBDQJKV-UHFFFAOYSA-N 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- YVPJCJLMRRTDMQ-UHFFFAOYSA-N ethyl diazoacetate Chemical compound CCOC(=O)C=[N+]=[N-] YVPJCJLMRRTDMQ-UHFFFAOYSA-N 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 238000003780 insertion Methods 0.000 description 4
- 230000037431 insertion Effects 0.000 description 4
- 238000006303 photolysis reaction Methods 0.000 description 4
- 230000015843 photosynthesis, light reaction Effects 0.000 description 4
- 238000005979 thermal decomposition reaction Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- MVLVMROFTAUDAG-UHFFFAOYSA-N ethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC MVLVMROFTAUDAG-UHFFFAOYSA-N 0.000 description 2
- 238000001030 gas--liquid chromatography Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000007791 liquid phase Substances 0.000 description 2
- YCOZIPAWZNQLMR-UHFFFAOYSA-N pentadecane Chemical compound CCCCCCCCCCCCCCC YCOZIPAWZNQLMR-UHFFFAOYSA-N 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 2
- MDQIOLAUIAZMHB-UHFFFAOYSA-N 3-heptylundecanoic acid Chemical compound CCCCCCCCC(CCCCCCC)CC(=O)O MDQIOLAUIAZMHB-UHFFFAOYSA-N 0.000 description 1
- BXEFQPCKQSTMKA-UHFFFAOYSA-N OC(=O)C=[N+]=[N-] Chemical compound OC(=O)C=[N+]=[N-] BXEFQPCKQSTMKA-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 210000000481 breast Anatomy 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- JRHHPGDCUCJQKX-UHFFFAOYSA-N ethyl 3-methylheptadecanoate Chemical compound CCCCCCCCCCCCCCC(C)CC(=O)OCC JRHHPGDCUCJQKX-UHFFFAOYSA-N 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 238000010574 gas phase reaction Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 150000002561 ketenes Chemical class 0.000 description 1
- 238000004949 mass spectrometry Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB3786167 | 1967-08-17 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1793209A1 true DE1793209A1 (de) | 1972-02-03 |
Family
ID=10399539
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19681793209 Pending DE1793209A1 (de) | 1967-08-17 | 1968-08-16 | Verzweigtkettige,aliphatische Ester und Verfahren zu ihrer Herstellung |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE719588A (https=) |
| DE (1) | DE1793209A1 (https=) |
| FR (1) | FR1576240A (https=) |
| GB (1) | GB1239394A (https=) |
| NL (1) | NL6811664A (https=) |
| SE (1) | SE354648B (https=) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1710225A4 (en) | 2004-01-28 | 2008-01-16 | Idemitsu Kosan Co | CARBONYL COMPOUND WITH LOW-CHAIN, BRANCHED ALKYL GROUP |
-
1967
- 1967-08-17 GB GB1239394D patent/GB1239394A/en not_active Expired
-
1968
- 1968-08-13 FR FR1576240D patent/FR1576240A/fr not_active Expired
- 1968-08-16 BE BE719588D patent/BE719588A/xx unknown
- 1968-08-16 DE DE19681793209 patent/DE1793209A1/de active Pending
- 1968-08-16 NL NL6811664A patent/NL6811664A/xx unknown
- 1968-08-19 SE SE1112468A patent/SE354648B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6811664A (https=) | 1969-02-19 |
| GB1239394A (https=) | 1971-07-14 |
| BE719588A (https=) | 1969-02-17 |
| SE354648B (https=) | 1973-03-19 |
| FR1576240A (https=) | 1969-07-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE69132892T2 (de) | Verfahren zur Herstellung von 4-Hydroxystyrol | |
| DE2834795A1 (de) | Verfahren zur herstellung von 2-(perfluoralkyl)-aethanolen | |
| DE2944295C2 (de) | Verfahren zur Herstellung von racemischer p-Hydroxy-Mandelsäure | |
| DE2437882B2 (de) | Verfahren zur herstellung von estern des 3-phenoxybenzylalkohols | |
| DE1793209A1 (de) | Verzweigtkettige,aliphatische Ester und Verfahren zu ihrer Herstellung | |
| DE2211436A1 (de) | Verfahren zur Herstellung von 2-Alkoxy-5-methoxybenzaldehyden | |
| EP0294774A3 (de) | Verfahren zur Herstellung von Gamma-Halogen-tiglinsäurealkylestern sowie deren Weiterverarbeitung zu 0,0-Dialkyl-Gamma-phosphono-tiglin-säurealkylestern | |
| CH631146A5 (de) | Verfahren zur herstellung von 2,6-dimethoxy-4-(quaternaeren-alkyl)phenolen. | |
| DE2636278A1 (de) | Verfahren zur herstellung von dialkylketalen | |
| DE885846C (de) | Verfahren zur Herstellung von Alkoholen der Acetylenreihe | |
| DE2050401A1 (de) | Neue Präparate zur Insektenbekämpfung und Verfahren zu ihrer Herstellung | |
| DE888736C (de) | Verfahren zur Herstellung hochwirksamer Trockenstoffkombinationen | |
| DE1768503C3 (de) | Verfahren zur Herstellung von Dimethylthiophosphit bzw. von Niederalkylthiophosphonigsäure-O-monomethylestern | |
| DE892893C (de) | Verfahren zur Herstellung von Carbonsaeureestern | |
| DE2363573A1 (de) | Verfahren zur herstellung eines mercaptocarbonsaeureesters | |
| DE919887C (de) | Verfahren zur Gewinnung hoehermolekularer Alkohole aus Gemischen mit Kohlenwasserstoffen | |
| DE727205C (de) | Verfahren zur Herstellung von Sulfinsaeuren | |
| DE1768930C3 (de) | Verfahren zur Herstellung von Cyclopent-2-enyl-phenolen | |
| DE857353C (de) | Verfahren zur Chlormethylierung von Alkylbenzolen | |
| DE851184C (de) | Verfahren zur Herstellung ungesaettigter Fettsaeuren | |
| DE923426C (de) | Verfahren zur Herstellung von ª‡-substituierten ª‰-Oxypropionsaeuren | |
| DE3225605A1 (de) | Verfahren zur herstellung von cyclopropanderivaten | |
| DE835140C (de) | Verfahren zur Herstellung organischer Persaeureester aus Hydroperoxyden | |
| DE2551598C2 (de) | Verfahren zur Herstellung von Alkanphosphonsäureestern | |
| DE2264501C3 (de) | Sulfone und Verfahren zu deren Herstellung |