CH123103A - Process for the preparation of the 1- (3'-sulfophenyl) -5-pyrazolone-3-carboxylic acid ethyl ester. - Google Patents
Process for the preparation of the 1- (3'-sulfophenyl) -5-pyrazolone-3-carboxylic acid ethyl ester.Info
- Publication number
- CH123103A CH123103A CH123103DA CH123103A CH 123103 A CH123103 A CH 123103A CH 123103D A CH123103D A CH 123103DA CH 123103 A CH123103 A CH 123103A
- Authority
- CH
- Switzerland
- Prior art keywords
- sulfophenyl
- pyrazolone
- carboxylic acid
- ethyl ester
- acid ethyl
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung des 1-(3'-Sulfophenyl)-6-pyrazolon-3-karbonsäureäthylesters. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung des 1-(3'-Sulfo- phenyl) - 5 - pyrazolon - 3 - karbonsäureäthyl- esters. Das Verfahren ist dadurch gekenn zeichnet, dass man das aus meta-Sulfophenyl- hydnazin und einem Salz des Oxalessigäthyl- esters erhältliche Hydra.zon in wässeriger Lösung erwärmt.
<I>Beispiel:</I> 188 Teile meta-Sulfophenylhydrazin wer= den in 1000 Teilen Wasser suspendiert; dazu setzt man 230 Teile des Natriumsalzes des Oxalessigäthylesters und lässt etwa 1 Stunde in der Kälte stehen; dann erhitzt man das Gemisch langsam zum Sieden; nach etwa 1 bis 2 Stunden beginnt die Lösung unter Ab scheidung von Kristallen zu stossen. Dann gibt man soviel Wasser hinzu, dass wieder in der Hitze eine klare Lösung entsteht und hält noch 1 bis 2 Stunden im Sieden.
Beim Erkalten kristallisiert der Sulf ophenylpyra- zolonkarbonsäureäthylester aus; durch Zu- Satz von verdünnten Säuren kann aus der Lauge noch eine weitere Menge an Ester er halten werden. Das so erhaltene Produkt kann durch Umkristallisieren aus Wasser gereinigt werden und stellt dann ein weisses Pulver dar. Es soll zur Darstellung von Farbstoffen die nen. -
Process for the preparation of the 1- (3'-sulfophenyl) -6-pyrazolone-3-carboxylic acid ethyl ester. The subject of this additional patent is a process for the preparation of 1- (3'-sulfophenyl) -5-pyrazolone-3-carboxylic acid ethyl ester. The process is characterized in that the hydra.zone obtainable from meta-sulfophenylhydnazine and a salt of oxaloacetic ethyl ester is heated in an aqueous solution.
<I> Example: </I> 188 parts of meta-sulfophenylhydrazine are suspended in 1000 parts of water; 230 parts of the sodium salt of the ethyl oxaloacetate are added and the mixture is left to stand in the cold for about 1 hour; then the mixture is slowly heated to boiling; after about 1 to 2 hours, the solution begins to poke with separation of crystals. Then add enough water that a clear solution is formed again in the heat and it is kept boiling for 1 to 2 hours.
On cooling, the ethyl sulfophenylpyrazolonecarboxylate crystallizes out; 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 is then 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 |
---|---|---|---|
DE123103X | 1924-11-27 | ||
CH119718T | 1925-11-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH123103A true CH123103A (en) | 1927-10-17 |
Family
ID=25709309
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH123103D CH123103A (en) | 1924-11-27 | 1925-11-24 | Process for the preparation of the 1- (3'-sulfophenyl) -5-pyrazolone-3-carboxylic acid ethyl ester. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH123103A (en) |
-
1925
- 1925-11-24 CH CH123103D patent/CH123103A/en unknown
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