CH222468A - 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
- CH222468A CH222468A CH222468DA CH222468A CH 222468 A CH222468 A CH 222468A CH 222468D A CH222468D A CH 222468DA CH 222468 A CH222468 A CH 222468A
- Authority
- CH
- Switzerland
- Prior art keywords
- condensation product
- nitrogen
- containing condensation
- production
- sulfuric acid
- 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
- C09B5/002—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being condensed in peri position and in 1-2 or 2-3 position
- C09B5/008—Dyes with an anthracene nucleus condensed with one or more heterocyclic rings with or without carbocyclic rings the heterocyclic rings being condensed in peri position and in 1-2 or 2-3 position only N-containing hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
<B>Zusatzpatent</B> zum Hauptpatent Nr. 218368. Verfahren zur Herstellung eines stickstoffhaltigen Kondensationsproduktes. Es wurde gefunden, dass ein stickstoff haltiges Kondensationsprodukt hergestellt werden kann, wenn man auf das Kondensa- tionsprodukt aus, 1 Mol 2,8-Dibromchrysen und 2 Mol 5-Amine-1,9-anthrapyrimidin kon densierende Mittel einwirken lässt.
Das stickstoffhaltige Kondensationspro- dukt bildet ein dunkles Pulver, das sich in konzentrierter Schwefelsäure mit schmutzig violetter Farbe, löst und Baumwolle aus brau ner Küpe in echten, braunen, Tönen färbt.
Die Einwirkung kondensierender Mittel, die oxydierend wirken können, wie z. B. A.luminiumcblarid, gegebenenfalls in Gegen wart organischer Säurechloride und von Verdünnungs- 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 Ka.rbazolringe gebildet.
Das neue stickstoffhaltige Kondensations produkt kann durch ein- oder mehrmaliges Kristallisieren aus organischen 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> 1 Teil des Kondensationsproduktes aus 1 Mol 2,8-Dibromchrysen und 2 Mol 5-Amino- 1,9-anthrapyrimidin werden bei 0-5 in 18 Teile Sähwef elsäure 96%ig eingetragen und 16 Stunden bei 0=5 gerührt. Nun trägt man in FEils, .gibt etwa 0,4 Teile Natrium nitrit zu und rührt 5 Stunden kräftig.
Die Reaktion ist nun beendet und der in sehr guter Ausbeute erhaltene Farbstoff kann ab filtriert, gewaschen und getrocknet werden.
<B> Additional patent </B> to main patent no. 218368. Process for the production of a nitrogen-containing condensation product. It has been found that a nitrogen-containing condensation product can be produced if the condensation product of 1 mol of 2,8-dibromochrysenic and 2 mol of 5-amine-1,9-anthrapyrimidine condensing agents is allowed to act.
The nitrogen-containing condensation product forms a dark powder which dissolves in concentrated sulfuric acid with a dirty purple color and dyes cotton from a brown vat in real, brown tones.
The action of condensing agents that can have an oxidizing effect, such as. B. A.luminiumcblarid, optionally in the presence of organic acid chlorides and diluents or solvents, can be carried out at a higher or lower temperature. Sulfuric acid and its derivatives, which are expediently applied at low temperature, are particularly suitable as condensing agents. Ka.rbazole rings are very likely to be formed on exposure to condensing agents.
The new nitrogen-containing condensation product can be crystallized one or more times from organic solvents or by treatment with oxydie-generating agents, such as. B. Alkali nitrite solution in acidic medium, alkali hyp @ chlorite solution or perborate solution.
<I> Example: </I> 1 part of the condensation product from 1 mol of 2,8-dibromochrysenic and 2 mol of 5-amino-1,9-anthrapyrimidine are added to 18 parts of 96% sulfuric acid at 0-5 and for 16 hours stirred at 0 = 5. Now you carry in parts, add about 0.4 parts of sodium nitrite and stir vigorously for 5 hours.
The reaction has now ended and the dye obtained in very good yield can be filtered off, washed and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH222468T | 1937-06-21 | ||
CH218368T | 1938-11-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH222468A true CH222468A (en) | 1942-07-15 |
Family
ID=25726159
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH222468D CH222468A (en) | 1937-06-21 | 1937-06-21 | Process for the production of a nitrogen-containing condensation product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH222468A (en) |
-
1937
- 1937-06-21 CH CH222468D patent/CH222468A/en unknown
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