DE273321C - - Google Patents
Info
- Publication number
- DE273321C DE273321C DENDAT273321D DE273321DA DE273321C DE 273321 C DE273321 C DE 273321C DE NDAT273321 D DENDAT273321 D DE NDAT273321D DE 273321D A DE273321D A DE 273321DA DE 273321 C DE273321 C DE 273321C
- Authority
- DE
- Germany
- Prior art keywords
- ester
- acetoacetic
- aminobenzoic acid
- acid esters
- parts
- 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
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 4
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical class NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- -1 benzyl ester Chemical class 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- 150000005415 aminobenzoic acids Chemical class 0.000 description 1
- BLFLLBZGZJTVJG-UHFFFAOYSA-N benzocaine Chemical compound CCOC(=O)C1=CC=C(N)C=C1 BLFLLBZGZJTVJG-UHFFFAOYSA-N 0.000 description 1
- DAOPOOMCXJPWPK-UHFFFAOYSA-N benzyl 4-aminobenzoate Chemical compound C1=CC(N)=CC=C1C(=O)OCC1=CC=CC=C1 DAOPOOMCXJPWPK-UHFFFAOYSA-N 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
- 238000009835 boiling Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 239000000543 intermediate Substances 0.000 description 1
- LZXXNPOYQCLXRS-UHFFFAOYSA-N methyl 4-aminobenzoate Chemical compound COC(=O)C1=CC=C(N)C=C1 LZXXNPOYQCLXRS-UHFFFAOYSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE273321C true DE273321C (cs) |
Family
ID=529787
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT273321D Active DE273321C (cs) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE273321C (cs) |
-
0
- DE DENDAT273321D patent/DE273321C/de active Active
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE273321C (cs) | ||
| DE1122075B (de) | Verfahren zur Herstellung von Aminoaryl-(thio)-phosphorsaeure-Derivaten | |
| DE1129153B (de) | Verfahren zur Herstellung von ª-Cyan-ª-Alkyl-ª-phenylacrylsaeureestern | |
| EP0008102A1 (de) | Verfahren zur Herstellung von Azaspirodecanen | |
| EP0352504A1 (de) | Verfahren zur gemeinschaftlichen Herstellung von 3-Dialkylaminopropionitrilen, Bis-(2-cyanoethyl)-ether und gewünschtenfalls Ethylencyanhydrin | |
| EP0144885A2 (de) | Verfahren zur gleichzeitigen Herstellung von Nitrilen und Acrylamid bzw. Methacrylamid | |
| DE2036681A1 (de) | Verfahren zur Herstellung von Nitro ximen | |
| EP0070424B1 (de) | Verfahren zur Herstellung von N,N'-disubstituierten 3-Aminopropanamiden | |
| EP0685456B1 (de) | Bisquartäre Ammoniumverbindungen des 2,2'-Dimethyl-1,1'-binaphtyls und Verfahren zu deren Herstellung | |
| DE252642C (cs) | ||
| DE521621C (de) | Verfahren zur Darstellung von Tetrahydronaphthochinonen | |
| DE568759C (de) | Verfahren zur Darstellung von 2-Methyl-5-oxypiperidin | |
| DE1643985C3 (de) | S-lsopropyl^nitro-phenyl-dimethyl-carbinol und 3,5-Diisopropyl-4-nitro-phenyldimethylcarbinol und Verfahren zu deren Herstellung | |
| DE2115944A1 (de) | Verfahren zur Herstellung von o Sulfobenzimiden | |
| DE222809C (cs) | ||
| DE1215154B (de) | Verfahren zur Herstellung von als Polymerisationsinhibitoren verwendbaren, olefinisch ungesaettigten Methylen-carbonamid-sulfonamiden | |
| DE283537C (cs) | ||
| EP0294686B1 (de) | Verfahren zur Herstellung von Iminokohlensäurediarylestern | |
| DE182783C (cs) | ||
| DE930686C (de) | Verfahren zur Herstellung von Dehydracetsaeure | |
| DE1470170C (cs) | ||
| DE942810C (de) | Verfahren zur Herstellung von ungesaettigten Ketonitrilen | |
| DE555240C (de) | Verfahren zur Herstellung von Pyridin- und Piperidinalkinen | |
| DE586068C (de) | Verfahren zur Darstellung von stickstoffhaltigen Derivaten des Anthracens | |
| DE1092919B (de) | Verfahren zur Herstellung von ungesaettigen 6gliedrigen Lactamen |