CH137941A - 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
- CH137941A CH137941A CH137941DA CH137941A CH 137941 A CH137941 A CH 137941A CH 137941D A CH137941D A CH 137941DA CH 137941 A CH137941 A CH 137941A
- Authority
- CH
- Switzerland
- Prior art keywords
- pyrazolanthrone
- preparation
- potash
- descendant
- halobenzanthrone
- Prior art date
Links
- ACPOUJIDANTYHO-UHFFFAOYSA-N anthra[1,9-cd]pyrazol-6(2H)-one Chemical compound C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=NNC2=C1 ACPOUJIDANTYHO-UHFFFAOYSA-N 0.000 title claims description 7
- 238000000034 method Methods 0.000 title claims description 7
- 238000002360 preparation method Methods 0.000 title claims description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 5
- 229940072033 potash Drugs 0.000 claims description 4
- 235000015320 potassium carbonate Nutrition 0.000 claims description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
- 238000002844 melting Methods 0.000 claims description 2
- 230000008018 melting Effects 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 claims 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- XYKSCLIHMGLNHK-UHFFFAOYSA-N 2-chlorobenzo[b]phenalen-7-one Chemical compound C1=CC2=CC(Cl)=CC(C=3C(=CC=CC=3)C3=O)=C2C3=C1 XYKSCLIHMGLNHK-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000984 vat dye Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B5/00—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings
- C09B5/02—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic ring being only condensed in peri position
- C09B5/04—Pyrazolanthrones
- C09B5/06—Benzanthronyl-pyrazolanthrone condensation products
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Darstellung eines Abkömmlings des Pyrazolanthrons. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung eines Benzantbronyl-pyrazolanthrons der Formel:
EMI0001.0004
bestehend in der Kondensation von Pyrazol- anthron, 2-Halogenbenzanthron und Pott asche.
Das Produkt findet für die Dar stellung von Küpenfarbstoffen Verwendung. <I>Beispiel:</I> Aus 22 Gewichtsteilen Pyrazolanthron und 22 Gewichtsteilen Pottasche wird durch Erhitzen in Nitrobenzol unter Rühren das Kalisalz des Pyrazolanthrüns gebildet. Nun werden 26,5 Gewichtsteile 2-Chlorbenzan- thron zugegeben und die Masse während etwa 10 Stunden bei Kochtemperatur weite verrührt. Nach dem Erkalten wird filtriert, mit Nitrobenzol, Alkohol und Wasser ge waschen und getrocknet. Das ;so. gebildete 2-Benzanthronyl-py-l-pyrazolanthron stellt ein gelbes.
Kristallpulver dar, das bei 398 bis 400' C schmilzt und sich in konzen trierter Schwefelsäure mit gelbroter Farbe löst. Im Gemisch mit dem isomeren und dem Verfahren des Patentes Nr. 136553 erhaltenen Bz-1-Benzanthronyl-py-l-pyrazol- anthron von ähnlichen Eigenschaften er fährt der Schmelzpunkt eine wesentliche De nression.
Process for the preparation of a descendant of the pyrazolanthrone. The present invention relates to a process for the preparation of a benzantbronylpyrazolanthrone of the formula:
EMI0001.0004
consisting of the condensation of pyrazole anthrone, 2-halobenzanthrone and potash.
The product is used for the presentation of vat dyes. <I> Example: </I> The potash salt of pyrazole anthrone is formed from 22 parts by weight of pyrazole anthrone and 22 parts by weight of potash by heating in nitrobenzene with stirring. Now 26.5 parts by weight of 2-chlorobenzanthrone are added and the mass is further stirred for about 10 hours at the boiling temperature. After cooling, it is filtered, washed with nitrobenzene, alcohol and water and dried. That so. formed 2-benzanthronyl-py-l-pyrazolanthrone represents a yellow.
Crystal powder is that melts at 398 to 400 'C and dissolves in concentrated sulfuric acid with a yellow-red color. When mixed with the isomeric and the process of Patent No. 136553 obtained Bz-1-benzanthronyl-py-l-pyrazol-anthrone of similar properties, the melting point experiences a substantial de nression.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH133473T | 1927-10-22 | ||
CH137941T | 1927-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH137941A true CH137941A (en) | 1930-01-31 |
Family
ID=25712070
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH137941D CH137941A (en) | 1927-10-22 | 1927-10-22 | Process for the preparation of a descendant of the pyrazolanthrone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH137941A (en) |
-
1927
- 1927-10-22 CH CH137941D patent/CH137941A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH137941A (en) | Process for the preparation of a descendant of the pyrazolanthrone. | |
DE921265C (en) | Process for the preparation of aryl-substituted pyrazoline compounds | |
CH136553A (en) | Process for the preparation of a descendant of the pyrazolanthrone. | |
DE490187C (en) | Process for the preparation of derivatives of benzanthrone | |
DE346188C (en) | Process for the preparation of 1-amino-2-anthraquinone aldehyde | |
CH136554A (en) | Process for the preparation of a descendant of the pyrazolanthrone. | |
DE550706C (en) | Process for the preparation of benzanthrones substituted in the benzene nucleus | |
DE495116C (en) | Process for the production of black and gray dyes of the benzanthrone series | |
CH136555A (en) | Process for the preparation of a descendant of the pyrazolanthrone. | |
DE701657C (en) | Process for the preparation of dinaphthinedione diketimide | |
DE539331C (en) | Process for the preparation of 3-oxythionaphthene-7-carboxylic acid chlorides or carboxylic acids | |
CH123853A (en) | Process for the production of bisaminotolylanthrone. | |
CH126194A (en) | Process for the preparation of a benzobenzanthronecarboxylic acid. | |
CH205063A (en) | Process for the preparation of terephthaloyl-1-anilide-4-chloride. | |
CH136556A (en) | Process for the preparation of a descendant of the pyrazolanthrone. | |
CH139365A (en) | Process for the preparation of a descendant of the pyrazolanthrone. | |
CH136546A (en) | Process for the preparation of a descendant of the pyrazolanthrone. | |
CH125474A (en) | Process for the preparation of methylpyrazolanthrone. | |
CH122359A (en) | Process for the preparation of bis-aminophenylanthrone. | |
CH201953A (en) | Process for the preparation of terephthaloyl 1- (4'-nitranilide) -4-chloride. | |
CH135114A (en) | Process for the preparation of an orange-colored vat dye of the anthanthrone series. | |
CH280186A (en) | Process for the production of a vat dye. | |
CH201179A (en) | Process for the preparation of an azole compound. | |
CH154067A (en) | Process for the preparation of 6- (nitro-6'-methylbenzthiazolyl-2 ') -4-amino-quinaldine. | |
CH127126A (en) | Process for the preparation of derivatives of barbituric acid. |