BE455368A - - Google Patents
Info
- Publication number
- BE455368A BE455368A BE455368DA BE455368A BE 455368 A BE455368 A BE 455368A BE 455368D A BE455368D A BE 455368DA BE 455368 A BE455368 A BE 455368A
- Authority
- BE
- Belgium
- Prior art keywords
- parts
- derivatives
- amides
- alkyleneimines
- alpha
- Prior art date
Links
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 150000001408 amides Chemical class 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- GRDLKEBELMXBIA-UHFFFAOYSA-N 2,2-dichloro-n-methylideneacetamide Chemical compound ClC(Cl)C(=O)N=C GRDLKEBELMXBIA-UHFFFAOYSA-N 0.000 description 1
- ATGFZSOBDDZEEX-UHFFFAOYSA-N 2-chloro-3-hydroxypropanamide Chemical compound NC(=O)C(Cl)CO ATGFZSOBDDZEEX-UHFFFAOYSA-N 0.000 description 1
- UMDRJSLGRKUJST-UHFFFAOYSA-N 2-chloro-N-methyl-N-octadecylacetamide Chemical compound CN(C(CCl)=O)CCCCCCCCCCCCCCCCCC UMDRJSLGRKUJST-UHFFFAOYSA-N 0.000 description 1
- TXNSZCSYBXHETP-UHFFFAOYSA-N 2-chloro-n-(hydroxymethyl)acetamide Chemical compound OCNC(=O)CCl TXNSZCSYBXHETP-UHFFFAOYSA-N 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000764773 Inna Species 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 description 1
- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical class OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- -1 halogen hydrates Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D203/00—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom
- C07D203/04—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D203/06—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D203/08—Heterocyclic compounds containing three-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring nitrogen atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE455368A true BE455368A (en:Method) |
Family
ID=109297
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE455368D BE455368A (en:Method) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE455368A (en:Method) |
-
0
- BE BE455368D patent/BE455368A/fr unknown
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| BE455368A (en:Method) | ||
| CN101323567A (zh) | 制备肉桂酸酯及其衍生物的方法 | |
| CH615902A5 (en) | Process for the preparation of substituted anilines | |
| FR2803846A1 (fr) | 3-(1-hydroxy-pentylidene)-5-nitro-3h-benzofuran-2-one, son procede de preparation et son utilisation | |
| EP0091851A1 (fr) | Procédé de préparation d'éthers d'aryle portant des substituants différents sur les deux noyaux aromatiques | |
| EP0037327B1 (fr) | Nouveaux dérivés substitués de l'acide 3-formyl 4-méthyl pentanoique, leur préparation et leur application à la préparation d'acide 3-formyl but-3-èn-1-oique substitué | |
| CH616659A5 (en:Method) | ||
| EP0066484B1 (fr) | Procédé de préparation d'imides N-benzylsubstitués | |
| FR2742143A1 (fr) | Procede de fabrication de fluoroalcanols | |
| BE817776Q (fr) | Nouveaux derives de 5-phenyl-tetrazoles | |
| FR2553762A1 (fr) | 1,3-bis(3-aminophenoxy)-5-halogenobenzenes et leur procede de preparation | |
| JPS5837299B2 (ja) | ２− ニトロベンズアルデヒドノ セイゾウホウ | |
| EP0148666B1 (fr) | Procédé de préparation de l'acide hydroxy-3 méthyl-3 glutarique | |
| BE856317Q (fr) | Procede de preparation d'acides arylalcanoiques | |
| BE480259A (en:Method) | ||
| BE632687A (en:Method) | ||
| BE562880A (en:Method) | ||
| BE561910A (en:Method) | ||
| BE476170A (en:Method) | ||
| WO2000047590A1 (fr) | Tris [(1h,1h, 2h,2h-perfluoroalkyl) aryl]phosphites et leurs applications en catalyse | |
| CH279831A (fr) | Procédé de préparation de ptéroylglutamate diisopropylique. | |
| BE569987A (en:Method) | ||
| CH362407A (fr) | Procédé de préparation d'(amino-2'-éthyl-1')-1-cyclohexéne-1-ones-3 N-disubstituées | |
| CH544753A (fr) | Nouveau procédé de préparation de pyrrolidines substituées | |
| CH279833A (fr) | Procédé de préparation de ptéroylglutamate dibenzylique. |