CH123102A - Process for the preparation of 1- (4'-sulfophenyl) -5-pyrazolone-3-carboxylic acid methyl ester. - Google Patents
Process for the preparation of 1- (4'-sulfophenyl) -5-pyrazolone-3-carboxylic acid methyl ester.Info
- Publication number
- CH123102A CH123102A CH123102DA CH123102A CH 123102 A CH123102 A CH 123102A CH 123102D A CH123102D A CH 123102DA CH 123102 A CH123102 A CH 123102A
- Authority
- CH
- Switzerland
- Prior art keywords
- methyl ester
- sulfophenyl
- carboxylic acid
- acid methyl
- pyrazolone
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung des 1-(4'-Sulfophenyl)-5-pyrazolon-3-karbonsäuremethylesters. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung des 1-(4'-Sulfo- phenyl) - 5 - pyrazolon - 3 - karb onsäuremethyl- esters. Das Verfahren ist dadurch gekenn zeichnet, dass man das aus p-Sulf ophenyl- hydrazin und einem Salz des Oxalessig- methylesters erhältliche Hydrazon in wässe riger Lösung erwärmt.
Beispiel: 188 Teile p-Sulfophenylhydrazin werden in 1000 Teilen Wasser suspendiert; dazu setzt man 202 Teile des Natriumsalzes des Oxalessigmethylesters und lässt etwa eine Stunde in der gälte stehen; dann erhitzt man das Gemisch langsam zum Sieden; nach etwa 1 bis 2 Stunden beginnt die Lösung un ter Abscheidung von Kristallen zu stossen. Dann gibt man soviel Wasser hinzu, dass wieder in der Hitze eine klare Lösung ent steht und hält noch 1 bis 2 Stunden im Sie den.
Beim Erkalten kristallisiert der Sulfo- phenylpyrazolonkarbonsäuremethylester aus; durch Zusatz von verdünnten Säuren kann aus der Lauge noch eine weitere Menge an Ester erhalten werden. Das so erhaltene Pro dukt kann durch Umkristallisieren aus Was ser gereinigt werden und stellt dann .ein weisses Pulver dar. Es soll zur Darstellung von Farbstoffen dienen.
Process for the preparation of 1- (4'-sulfophenyl) -5-pyrazolone-3-carboxylic acid methyl ester. The subject of this additional patent is a process for the preparation of 1- (4'-sulfophenyl) - 5 - pyrazolone - 3 - carbonic acid methyl ester. The process is characterized in that the hydrazone obtainable from p-sulfophenylhydrazine and a salt of the methyl oxaloacetate is heated in an aqueous solution.
Example: 188 parts of p-sulfophenylhydrazine are suspended in 1000 parts of water; 202 parts of the sodium salt of oxaloacetamethyl ester are added and the mixture is left to stand in the cold for about an hour; then the mixture is slowly heated to boiling; after about 1 to 2 hours the solution begins to collide with the separation of crystals. Then you add enough water that a clear solution is created again in the heat and it stays in the oven for another 1 to 2 hours.
The methyl sulfophenylpyrazolonecarboxylate crystallizes out on cooling; By adding dilute acids, a further amount of ester can be obtained from the lye. The product obtained in this way can be purified by recrystallization from water and then represents a white powder. It is intended to be used to represent dyes.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE123102X | 1924-11-27 | ||
CH119718T | 1925-11-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH123102A true CH123102A (en) | 1927-10-17 |
Family
ID=25709308
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH123102D CH123102A (en) | 1924-11-27 | 1925-11-24 | Process for the preparation of 1- (4'-sulfophenyl) -5-pyrazolone-3-carboxylic acid methyl ester. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH123102A (en) |
-
1925
- 1925-11-24 CH CH123102D patent/CH123102A/en unknown
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