BE572813A - - Google Patents
Info
- Publication number
- BE572813A BE572813A BE572813DA BE572813A BE 572813 A BE572813 A BE 572813A BE 572813D A BE572813D A BE 572813DA BE 572813 A BE572813 A BE 572813A
- Authority
- BE
- Belgium
- Prior art keywords
- carboxylic acids
- solvent
- reaction
- methylolmethacrylamide
- saturated
- Prior art date
Links
- 239000002904 solvent Substances 0.000 claims description 11
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 9
- 150000001735 carboxylic acids Chemical class 0.000 claims description 6
- 150000001299 aldehydes Chemical class 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- -1 methylol compound Chemical class 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 239000003849 aromatic solvent Substances 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- DNTMQTKDNSEIFO-UHFFFAOYSA-N n-(hydroxymethyl)-2-methylprop-2-enamide Chemical compound CC(=C)C(=O)NCO DNTMQTKDNSEIFO-UHFFFAOYSA-N 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 239000002002 slurry Substances 0.000 claims 2
- 229920001577 copolymer Polymers 0.000 claims 1
- 238000001035 drying Methods 0.000 claims 1
- 239000000155 melt Substances 0.000 claims 1
- 239000012188 paraffin wax Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical class NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 150000007514 bases Chemical class 0.000 description 1
- MLUCVPSAIODCQM-NSCUHMNNSA-N crotonaldehyde Chemical compound C\C=C\C=O MLUCVPSAIODCQM-NSCUHMNNSA-N 0.000 description 1
- MLUCVPSAIODCQM-UHFFFAOYSA-N crotonaldehyde Natural products CC=CC=O MLUCVPSAIODCQM-UHFFFAOYSA-N 0.000 description 1
- 150000001470 diamides Chemical class 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 150000002913 oxalic acids Chemical class 0.000 description 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/30—Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
- C07F9/32—Esters thereof
- C07F9/3258—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/3264—Esters with hydroxyalkyl compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Phenolic Resins Or Amino Resins (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BE572813A true BE572813A (enrdf_load_stackoverflow) |
Family
ID=190487
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BE572813D BE572813A (enrdf_load_stackoverflow) |
Country Status (1)
| Country | Link |
|---|---|
| BE (1) | BE572813A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1237102B (de) * | 1963-08-31 | 1967-03-23 | Basf Ag | Verfahren zur Herstellung von N, N'-(1, 2-Dihydroxyaethylen)-bis-carbonsaeureamiden durch Umsetzung von ungesaettigten Carbonsaeureamiden mit Glyoxal |
-
0
- BE BE572813D patent/BE572813A/fr unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1237102B (de) * | 1963-08-31 | 1967-03-23 | Basf Ag | Verfahren zur Herstellung von N, N'-(1, 2-Dihydroxyaethylen)-bis-carbonsaeureamiden durch Umsetzung von ungesaettigten Carbonsaeureamiden mit Glyoxal |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| FR2819808A1 (fr) | Compositions stabilisees d'acide o-iodoxybenzoique et leur procede de preparation | |
| BE572813A (enrdf_load_stackoverflow) | ||
| EP0004211B1 (fr) | Préparation du nitro-2 méthyl-2 propanol-1 | |
| FR2665897A1 (fr) | Procede de transformation de l'acide (benzoyl-3 phenyl)-2 propionique-r(-) en isomere s(+). | |
| BE448884A (enrdf_load_stackoverflow) | ||
| EP0184572B1 (fr) | Procédé de préparation d'acides alpha-hydroxy-alcanoiques | |
| FR2649098A1 (fr) | Polymeres chiraux pour la synthese d'aminoacides enantiomeriquement purs | |
| FR2486526A1 (fr) | Procede de preparation de derives de l'oxyde de diphenyle | |
| BE431257A (enrdf_load_stackoverflow) | ||
| EP1016652B1 (fr) | Procédé d'obtention de N-formyl-leucine de pureté élevée | |
| BE505023A (enrdf_load_stackoverflow) | ||
| EP1627872B1 (fr) | Procédé de synthèse du sel de potassium du dinitrobenzofuroxanne | |
| FR2686880A1 (fr) | Procede de preparation de la chloro-5 3h-benzofuranone-2 et son application a l'obtention de l'acide chloro-5 hydroxy-2 phenylacetique. | |
| LU82414A1 (fr) | Procede d'oxydation d'hydrocarbures | |
| BE587279A (enrdf_load_stackoverflow) | ||
| BE533042A (enrdf_load_stackoverflow) | ||
| FR2462421A1 (fr) | Procede de preparation du sel d'acide p-acetamidobenzoique d'un complexe inosine-dimethylaminoisopropanol | |
| CH411815A (fr) | Procédé de fabrication du dichlorodiphényltrichloréthane | |
| BE439587A (enrdf_load_stackoverflow) | ||
| EP0018931A1 (fr) | Préparation de benzoxazolone | |
| BE615918A (enrdf_load_stackoverflow) | ||
| BE439145A (enrdf_load_stackoverflow) | ||
| BE483465A (enrdf_load_stackoverflow) | ||
| BE505572A (enrdf_load_stackoverflow) | ||
| BE549627A (enrdf_load_stackoverflow) |