DE180202C - - Google Patents
Info
- Publication number
- DE180202C DE180202C DENDAT180202D DE180202DA DE180202C DE 180202 C DE180202 C DE 180202C DE NDAT180202 D DENDAT180202 D DE NDAT180202D DE 180202D A DE180202D A DE 180202DA DE 180202 C DE180202 C DE 180202C
- Authority
- DE
- Germany
- Prior art keywords
- methyl
- ethyl ether
- ketone
- acid
- chloromethyl ethyl
- 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.)
- Active
Links
- 150000002825 nitriles Chemical class 0.000 claims description 8
- FCYRSDMGOLYDHL-UHFFFAOYSA-N chloromethoxyethane Chemical compound CCOCCl FCYRSDMGOLYDHL-UHFFFAOYSA-N 0.000 claims description 7
- -1 Alkoxy glycol Chemical compound 0.000 claims description 6
- 150000002576 ketones Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 150000001408 amides Chemical class 0.000 claims description 5
- 238000006243 chemical reaction Methods 0.000 claims description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 150000002901 organomagnesium compounds Chemical class 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 2
- TVZPLCNGKSPOJA-UHFFFAOYSA-N copper zinc Chemical compound [Cu].[Zn] TVZPLCNGKSPOJA-UHFFFAOYSA-N 0.000 claims description 2
- 239000011777 magnesium Substances 0.000 claims description 2
- 229910052749 magnesium Inorganic materials 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 239000007858 starting material Substances 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims 5
- 239000007795 chemical reaction product Substances 0.000 claims 3
- 239000007859 condensation product Substances 0.000 claims 3
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 3
- 239000005457 ice water Substances 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- LSKONYYRONEBKA-UHFFFAOYSA-N 2-Dodecanone Chemical compound CCCCCCCCCCC(C)=O LSKONYYRONEBKA-UHFFFAOYSA-N 0.000 claims 2
- 241000208181 Pelargonium Species 0.000 claims 2
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 claims 2
- ZAJNGDIORYACQU-UHFFFAOYSA-N decan-2-one Chemical compound CCCCCCCCC(C)=O ZAJNGDIORYACQU-UHFFFAOYSA-N 0.000 claims 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 claims 2
- 239000000047 product Substances 0.000 claims 2
- VMKOFRJSULQZRM-UHFFFAOYSA-N 1-bromooctane Chemical compound CCCCCCCCBr VMKOFRJSULQZRM-UHFFFAOYSA-N 0.000 claims 1
- CXKAZTSHVRMSRT-UHFFFAOYSA-N 1-ethoxypropan-2-one Chemical compound CCOCC(C)=O CXKAZTSHVRMSRT-UHFFFAOYSA-N 0.000 claims 1
- WPYUCWSMVJJWFI-UHFFFAOYSA-N 2-ethoxyacetonitrile Chemical compound CCOCC#N WPYUCWSMVJJWFI-UHFFFAOYSA-N 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 239000006001 Methyl nonyl ketone Substances 0.000 claims 1
- 239000005643 Pelargonic acid Substances 0.000 claims 1
- KMPQYAYAQWNLME-UHFFFAOYSA-N Undecanal Natural products CCCCCCCCCCC=O KMPQYAYAQWNLME-UHFFFAOYSA-N 0.000 claims 1
- AGWLCKBNBSUOAZ-UHFFFAOYSA-N benzenesulfonic acid;hydrazine Chemical compound NN.OS(=O)(=O)C1=CC=CC=C1 AGWLCKBNBSUOAZ-UHFFFAOYSA-N 0.000 claims 1
- HRQGCQVOJVTVLU-UHFFFAOYSA-N bis(chloromethyl) ether Chemical compound ClCOCCl HRQGCQVOJVTVLU-UHFFFAOYSA-N 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000005998 bromoethyl group Chemical group 0.000 claims 1
- 239000003153 chemical reaction reagent Substances 0.000 claims 1
- 150000001804 chlorine Chemical class 0.000 claims 1
- 238000001816 cooling Methods 0.000 claims 1
- 238000000354 decomposition reaction Methods 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
- 150000002366 halogen compounds Chemical class 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 150000002496 iodine Chemical class 0.000 claims 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 230000004048 modification Effects 0.000 claims 1
- 238000012986 modification Methods 0.000 claims 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N noncarboxylic acid Natural products CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 claims 1
- 150000002902 organometallic compounds Chemical class 0.000 claims 1
- 238000010992 reflux Methods 0.000 claims 1
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 claims 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 claims 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/13—Saturated ethers containing hydroxy or O-metal groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE180202C true DE180202C (en:Method) |
Family
ID=444473
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT180202D Active DE180202C (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE180202C (en:Method) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1061765B (de) * | 1956-11-27 | 1959-07-23 | Rhone Poulenc Sa | Verfahren zur Herstellung von Glykolmonoaethern |
| US2916520A (en) * | 1959-12-08 | Production of glycol monoethers |
-
0
- DE DENDAT180202D patent/DE180202C/de active Active
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2916520A (en) * | 1959-12-08 | Production of glycol monoethers | ||
| DE1061765B (de) * | 1956-11-27 | 1959-07-23 | Rhone Poulenc Sa | Verfahren zur Herstellung von Glykolmonoaethern |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2139564B2 (de) | Verfahren zur Herstellung von 33'33'-Tetra-isopropyl-4,4'-hydroxydiphenyl | |
| DE2025662A1 (en:Method) | ||
| DE180202C (en:Method) | ||
| DE2443142C2 (de) | Verfahren zur Herstellung von Cyclopropancarbonsäurenitril | |
| EP0114359B1 (de) | Verfahren zur Herstellung von perfluoralkylsubstituierten carbocyclischen oder heterocyclischen Verbindungen | |
| EP0087585A1 (de) | Verfahren zur Herstellung von 3-Alkoxi-acrylnitrilen | |
| EP1070718B1 (de) | Verfahren zur Herstellung von Grignard-Reagenzien und neue Grignard-Reagenzien | |
| DE2451006A1 (de) | Extraktionsverfahren | |
| DE2840272A1 (de) | Verfahren zur herstellung von o-benzyltoluol und alkylderivaten desselben | |
| DE19935448B4 (de) | Verfahren zur Herstellung sekundärer aliphatischer Amine aus Aldehyden mittlerer Kettenlänge | |
| DE2327510B2 (de) | Verfahren zur Herstellung von Dimethylalkylaminen aus Aldehyd-Ammoniak-Verbindungen | |
| DE702894C (de) | Verfahren zur Herstellung von Oxyketonen | |
| DE1927528C3 (de) | Verfahren zur herstellung von alpha- aethinylaminen | |
| DE767192C (de) | Verfahren zur Herstellung von gesaettigten N-substituierten 2-Amino-alkanen | |
| WO2005019154A1 (de) | VERFAHREN ZUR HERSTELLUNG VON α-FLUOR-MALONSÄUREDIALKYLESTERN | |
| DE951933C (de) | Verfahren zur Herstellung von organischen Hydroxylaminverbindungen | |
| DE3120558A1 (de) | Verfahren zur reinigung von n,n-dimethylaminopropylamin | |
| DE119862C (en:Method) | ||
| DE2510571C2 (de) | Verfahren zur Herstellung ungesättigter Cyanocarbonylverbindungen | |
| DE189841C (en:Method) | ||
| DE881648C (de) | Verfahren zur Herstellung von gesaettigten ª‡, ªÏ-Dinitrilen | |
| DE102005057715A1 (de) | Prozess zur Herstellung symmetrischer und unsymmetrischer N,N-Dihydrocarbylhydroxylamine | |
| DE157840C (en:Method) | ||
| DE1568092C (de) | Verfahren zur Herstellung von neuen Derivaten des 5,10 Methano 5H dibenzo ecki ge Klammer auf a,d eckige Klammer zu cycloheptens | |
| AT229285B (de) | Verfahren zur Reduktion von Carbonylverbindungen |