CH222469A - Process for the production of a nitrogen-containing condensation product. - Google Patents
Process for the production of a nitrogen-containing condensation product.Info
- Publication number
- CH222469A CH222469A CH222469DA CH222469A CH 222469 A CH222469 A CH 222469A CH 222469D A CH222469D A CH 222469DA CH 222469 A CH222469 A CH 222469A
- Authority
- CH
- Switzerland
- Prior art keywords
- condensation product
- nitrogen
- containing condensation
- production
- yellow
- Prior art date
Links
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
- C09B5/24—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being only condensed with an anthraquinone nucleus in 1-2 or 2-3 position
- C09B5/26—Carbazoles of the anthracene series
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines stickstoffhaltigen Kondensationsproduktes. Es wurde gefunden, d:ass ein süekstoff- haltiges Kondensationsprodukt hergestellt werden kann, wenn man auf D'i-(5'-cinn- amoylamino-1'-anthrachinonyl-) 2,8-diamino- chrysen kondensierende Mittel einwirken lässt.
Das, stickstoffhaltige Kondensationspro- dukt färbt aus gel:b-roter Küpe Baumwolle in reinen -elbbraunen Tönen von hervorragen den Echtheiten.
Die Einwirkung kondensierender Mittel, die oxydierend wirken können, wie z. B. Aluminiumchlorid, gegebenenfalls in Gegen wart organischer Säurechloride und von Z erdünnungs- oder Lösungsmitteln, kann bei höherer oder niederer Temperatur erfolgen. Als Kondensationsmittel, besonders, geeignet. sind Schwefelsäure und ihre Derivate, die zweckmässig bei niederer Temperatur ange wandt werden. Sehr wahrscheinlich werden bei der Einwirkung kondensierender Mittel Karba.zolringe .gebildet.
Das neue stickstoffhaltige Kondensations produkt kann durch ein- oder mehrmaliges Kristallisieren aus arganischien Lösungs mitteln oder durch Behandlung mit oxydie renden Mitteln, wie z. B. Alkalinitritlösung in saurem Medium, Alkalihyp@ochloritlösung oder Perboratlösung, gereinigt werden.
<I>Beispiel:</I> 2 Teile Di-(5'-cinnamoylamino-t'=anthra- chinonyl-)2,8@diaminoehrysen werden bei 0 bis 5 in. 8,6 Teile 96%ige Schwefelsäure eingetragen und 20 Stunden bei dieser Tem peratur weiter gerührt. Zur Beendigung der Farbstoffbildung wird in Eis, -dem 0,6 Teile 1\Tatriumnitrit zugefügt wurden, eingetragen, 5 Stunden kräftig gerührt und hierauf ab filtriert, ausgewaschen und der Farbstoff mit Wasser angeteigt.
Process for the production of a nitrogen-containing condensation product. It has been found that a condensation product containing sweeteners can be produced if agents which condense D'i- (5'-cinnamoylamino-1'-anthraquinonyl) 2,8-diaminochrysenic are allowed to act.
The nitrogen-containing condensation product dyes from yellow: b-red vat cotton in pure yellow-brown tones with excellent fastness properties.
The action of condensing agents that can have an oxidizing effect, such as. B. aluminum chloride, optionally in the presence of organic acid chlorides and diluents or solvents, can be carried out at higher or lower temperature. Particularly suitable as a condensing agent. are sulfuric acid and its derivatives, which are expediently applied at low temperatures. It is very likely that the action of condensing agents will form karba.zol rings.
The new nitrogen-containing condensation product can medium by one or more times crystallization from arganic solvents or by treatment with oxydie-generating agents such. B. Alkali nitrite solution in acidic medium, alkali hyp @ chlorite solution or perborate solution.
<I> Example: </I> 2 parts of di- (5'-cinnamoylamino-t '= anthraquinonyl-) 2,8 @ diaminoehrysen are added at 0 to 5 in. 8.6 parts of 96% sulfuric acid and 20 Stirred for hours at this temperature. To terminate the formation of the dye, ice to which 0.6 part of sodium nitrite has been added is introduced, stirred vigorously for 5 hours and then filtered off, washed out and the dye made into a paste with water.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH222469T | 1937-06-21 | ||
CH218368T | 1938-11-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH222469A true CH222469A (en) | 1942-07-15 |
Family
ID=25726160
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH222469D CH222469A (en) | 1937-06-21 | 1937-06-21 | Process for the production of a nitrogen-containing condensation product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH222469A (en) |
-
1937
- 1937-06-21 CH CH222469D patent/CH222469A/en unknown
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