CH104014A - Process for the preparation of a condensation product of the anthraquinone series which can be used as dye and dye intermediate. - Google Patents
Process for the preparation of a condensation product of the anthraquinone series which can be used as dye and dye intermediate.Info
- Publication number
- CH104014A CH104014A CH104014DA CH104014A CH 104014 A CH104014 A CH 104014A CH 104014D A CH104014D A CH 104014DA CH 104014 A CH104014 A CH 104014A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- condensation product
- anthraquinone
- preparation
- nitrobenzene
- 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
- C09B5/34—Anthraquinone acridones or thioxanthrones
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung eines als Farbstoff und Farbstoffzwischenprodukt verwendbaren Kondensationsproduktes der Anthrachinonreihe. Es wurde gefunden, dass man ein neues, als Farbstoff und Farbstoffzwischenprodukt verwendbares Kondensationsprodukt der An- thrachinonreihe erhält, wenn man Cyanur- chlorid mit 1-Amino-4-methoxy-anthrachinon und 4-Amino-2.1-Anthrachinonakridon um setzt.
Beispiel: Eine Lösung von 18,5 Teilen Cyanur- chlorid in etwa 300 Teilen Nitrobenzol wird mit 34 Teilen 4 Amino-2.1-Anthrachinonakri- don während einer halben Stunde bei schwa chem Sieden des Nitrobenzols erhalten, dar nach wird erkalten gelassen und filtriert. Das so erhaltene feste Produkt wird in etwa 300 Teilen, vorteilhaft etwa 0,8"/o Diäthyl- anilin enthaltenden, Nitrobenzol aufgenommen.
Nach Zusatz von 25,3 Teilen 1-Amino-4- methoxy-anthrachinoi: -- \,#lischung wird diese während 10 Stunden auf 100 , sodann nach Zugabe von 20 Teilen calcinierter Soda wäh rend dreissig Stunden auf 120-12511 erwärmt, zweckmässig unter Rühren. Nach Erkalten wird das ausgeschiedene neue Kondensations produkt abfiltriert, gewaschen und getrocknet. Es stellt ein blauschwarzes Pulver dar, ist unlöslich in kaltem und heissem Wasser, sowie Alkohol, sehr schwer löslich in kaltem Chlor benzol und Nitrobenzol, schwer löslich in siedendem Chlorbenzol, ziemlich löslich in siedendem Nitrobenzol mit marineblauer Farbe.
Seine Lösung in konzentrierter Schwefelsäure ist braunrot. Es -liefert eine rote Küpe, aus der Baumwolle in grauen Tönen angefärbt wird.
Process for the preparation of a condensation product of the anthraquinone series which can be used as dye and dye intermediate. It has been found that a new condensation product of the anthraquinone series which can be used as dye and dye intermediate is obtained if cyanuric chloride is reacted with 1-amino-4-methoxy-anthraquinone and 4-amino-2,1-anthraquinone acridone.
Example: A solution of 18.5 parts of cyanuric chloride in about 300 parts of nitrobenzene is obtained with 34 parts of 4-amino-2,1-anthraquinone acridone over half an hour with the nitrobenzene boiling gently, after which it is allowed to cool and filtered. The solid product thus obtained is taken up in about 300 parts, advantageously about 0.8 "/ o diethylaniline-containing nitrobenzene.
After adding 25.3 parts of 1-amino-4-methoxy-anthraquinone: - \, # mixture this is heated to 100 for 10 hours, then after the addition of 20 parts of calcined soda for thirty hours to 120-12511, appropriate while stirring. After cooling, the precipitated new condensation product is filtered off, washed and dried. It is a blue-black powder, is insoluble in cold and hot water, as well as alcohol, very sparingly soluble in cold chlorobenzene and nitrobenzene, sparingly soluble in boiling chlorobenzene, fairly soluble in boiling nitrobenzene with a navy blue color.
Its solution in concentrated sulfuric acid is brownish red. It delivers a red vat from which cotton is dyed in gray tones.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH97059T | 1921-05-30 | ||
CH104014T | 1923-03-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH104014A true CH104014A (en) | 1924-03-17 |
Family
ID=25705201
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH104014D CH104014A (en) | 1921-05-30 | 1923-03-29 | Process for the preparation of a condensation product of the anthraquinone series which can be used as dye and dye intermediate. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH104014A (en) |
-
1923
- 1923-03-29 CH CH104014D patent/CH104014A/en unknown
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