CH219586A - Process for the preparation of a vat dye. - Google Patents
Process for the preparation of a vat dye.Info
- Publication number
- CH219586A CH219586A CH219586DA CH219586A CH 219586 A CH219586 A CH 219586A CH 219586D A CH219586D A CH 219586DA CH 219586 A CH219586 A CH 219586A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dye
- weight
- parts
- vat dye
- 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
- C09B5/28—Anthrimide carbazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. 214908. Verfahren zur Darstellung eines Nüpenfarbstoffes. Gegenstand dieses Patentes ist ein Verfah ren zur Herstellung eines güpenfarbstoffes, der pflanzliche Fasern in rotstichig braunen Tönen anfärbt. Das Verfahren zu seiner Her stellung besteht darin, dass man das Anthri-- mid der nachstehenden Formel
EMI0001.0008
mit sauren Kondensationsmitteln behandelt.
Der Farbstoff bildet ein dunkelbraunes Pulver, dessen rotbraune Hydrosulfitküpe zur pflanzlichen Faser grosse Affinität hat und letztere in sehr echten, klaren, rotstichig braunen Tönen färbt. <I>Beispiel:</I> 9 Gewichtsteile 5.5'-Diamino-1.1'-di- anthrimidcarbozol, 16 Gewichtsteile 4' . 6'- Dichloranthrachinon - 2. 1-N-1' . 2'-N - benz- acridon, 3 Gewichtsteile Pottasche, 0,5 Ge wichtsteile Kupferacetat und 200 Gewichts- teile Naphthalin werden 10 Stunden auf 210' C unter Rühren erhitzt.
Dann wird mit Chlorbenzol verdünnt, heiss abgesaugt und in üblicher Weise abgesaugt und getrocknet. Zur Kondensation werden 21 Gewichtsteile des Trianthrimides in eine Lösung von 70 Ge- wichtsteilen Aluminiumchlorid und 210 Ge wichtsteilen Nitrobenzol eingetragen und Stunden auf 90 " C erhitzt, worauf die Lö sungsfarbe von oliv nach grünblau umge schlagen ist. Das Nitrobenzol wird mit Was serdampf abgetrieben, der Farbstoff, der die nachstehende Konstitution besitzt
EMI0002.0004
in üblicher Weise isoliert, fein verteilt, mit. alkalischer Chlorlauge oxydiert, um ihn zu schönen, abgesaugt, gewaschen und getrock net.
Er bildet ein dunkelbraunes Pulver, des sen rotbraune Hydrosulfitküpe zur pflanz lichen Faser grosse Affinität hat und letztere in sehr echten, klaren rotstiehig braunen Tönen färbt.
Additional patent to main patent no. 214908. Process for the preparation of a pebble dye. The subject of this patent is a process for the production of a güpen dye that dyes vegetable fibers in reddish brown tones. The process for making it is by taking the anthrimide of the formula below
EMI0001.0008
treated with acidic condensing agents.
The dye forms a dark brown powder, the red-brown hydrosulphite vat of which has a great affinity for the vegetable fiber and colors the latter in very genuine, clear, reddish brown tones. <I> Example: </I> 9 parts by weight of 5.5'-diamino-1.1'-di-anthrimidecarbozole, 16 parts by weight of 4 '. 6'-dichloroanthraquinone - 2. 1-N-1 '. 2'-N-benz-acridone, 3 parts by weight of potash, 0.5 parts by weight of copper acetate and 200 parts by weight of naphthalene are heated to 210 ° C. for 10 hours while stirring.
It is then diluted with chlorobenzene, filtered off with suction while hot and suctioned off and dried in the usual way. For condensation, 21 parts by weight of the trianthrimide are added to a solution of 70 parts by weight of aluminum chloride and 210 parts by weight of nitrobenzene and heated to 90 ° C. for hours, whereupon the solution color has changed from olive to green-blue. The nitrobenzene is driven off with water vapor, the dye which has the following constitution
EMI0002.0004
isolated in the usual way, finely divided, with. alkaline chlorine hydroxide is oxidized in order to make it beautiful, suctioned off, washed and dried.
It forms a dark brown powder, the reddish brown hydrosulphite vat of which has a great affinity for the vegetable fiber and colors the latter in very genuine, clear reddish brown tones.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE219586X | 1938-05-27 | ||
CH214908T | 1939-05-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH219586A true CH219586A (en) | 1942-02-15 |
Family
ID=25725658
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH219586D CH219586A (en) | 1938-05-27 | 1939-05-19 | Process for the preparation of a vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH219586A (en) |
-
1939
- 1939-05-19 CH CH219586D patent/CH219586A/en unknown
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