CH136551A - Process for the preparation of a descendant of the pyrazolanthrone. - Google Patents
Process for the preparation of a descendant of the pyrazolanthrone.Info
- Publication number
- CH136551A CH136551A CH136551DA CH136551A CH 136551 A CH136551 A CH 136551A CH 136551D A CH136551D A CH 136551DA CH 136551 A CH136551 A CH 136551A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- acid
- preparation
- pyrazolanthrone
- descendant
- Prior art date
Links
Landscapes
- Medicinal Preparation (AREA)
Description
Verfahren zur Darstellung eines Abkömmlings des Pyrazolanthrons. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur D@arsteillung von Py-1- ss-Naphtylpyraz@ol@a.nthron-o-carbonsäure der Formel
EMI0001.0007
durch Kondensation von Pvrazolanthron mit 2-Chlor-3-naphtoesäure in \ Gegenwart eines säurebindenden Mittels. Die. Reaktion kann auch in Gegenwart einest Katalysators aus geführt werden.
Das erhaltene Produkt wird zur Darstellung von Küpenfarbstoffen ver wendet. <I>Beispiel:</I> 22 G. T. Pyrazola,nthron, 22 G. T. 2-Chlor- 3-naphtoesäure. 15 G. T. Kaliumacetat, 1 G. T. Kupferacetat und 0,5 G. T. Kupferpulver werden in 200 G. T. A.mylalko o1 unter Rüh ren zum Sieden erhitzt, bis die Umsetzung beendet ist.
Durch Wasserdampfdestillation wird der Amylajlkohol entfernt, der Rück stand in verdünnter Natriumcarbonatlösung gelöst, von etwa ungelöst bleibenden Teilen abfiltriert und das" gelbe Filtrat mit ver dünnter Mineralsäure gefällt. Die Py-1-ss- Naphty,Ipyrazoilaathro@n-o-e:arb-onsAure fällt als hellgelber Niederschlag aus und stellt naeh dem Trocknen ein hellgelbes Puler dar.
Sie schmilzt nach dem Umkristallisieren aus Eisessig bei 277 bis 279 'unter Aufschäumen. Die Lösungsfarbe in conc. Schwefelsäure ist orange.
Process for the preparation of a descendant of the pyrazolanthrone. The present invention relates to a process for the division of py-1-ss-naphthylpyraz @ ol @ a.nthrone-o-carboxylic acid of the formula
EMI0001.0007
by condensation of pvrazolanthrone with 2-chloro-3-naphthoic acid in the presence of an acid-binding agent. The. The reaction can also be carried out in the presence of a catalyst.
The product obtained is used for the preparation of vat dyes. <I> Example: </I> 22 G. T. Pyrazola, nthron, 22 G. T. 2-chloro-3-naphthoic acid. 15 G. T. potassium acetate, 1 G. T. copper acetate and 0.5 G. T. copper powder are heated to boiling in 200 G. T. A. mylalko o1 with stirring until the reaction is complete.
The amylajl alcohol is removed by steam distillation, the residue is dissolved in dilute sodium carbonate solution, any parts remaining undissolved are filtered off, and the yellow filtrate is precipitated with dilute mineral acid pale yellow precipitate and turns a pale yellow powder after drying.
After recrystallization from glacial acetic acid, it melts at 277 to 279 'with foaming. The solution color in conc. Sulfuric acid is orange.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE136551X | 1926-10-22 | ||
CH133473T | 1927-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH136551A true CH136551A (en) | 1929-11-15 |
Family
ID=25712076
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH136551D CH136551A (en) | 1926-10-22 | 1927-10-22 | Process for the preparation of a descendant of the pyrazolanthrone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH136551A (en) |
-
1927
- 1927-10-22 CH CH136551D patent/CH136551A/en unknown
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