CH120710A - Process for the preparation of monobromoisodibenzanthrone. - Google Patents
Process for the preparation of monobromoisodibenzanthrone.Info
- Publication number
- CH120710A CH120710A CH120710DA CH120710A CH 120710 A CH120710 A CH 120710A CH 120710D A CH120710D A CH 120710DA CH 120710 A CH120710 A CH 120710A
- Authority
- CH
- Switzerland
- Prior art keywords
- bzl
- preparation
- benzanthronyl
- sulfide
- monobromoisodibenzanthrone
- Prior art date
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von 1Ylonobromisoclibenzanthron. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur Darstellung von Monobrom- isodibenzanthron. Das Verfahren besteht darin, dass man Monobrom-Bzl, Bz1'-benzantlironylsulfid fol gender Formel:
EMI0001.0006
mit alkalischen Kondensationsmitteln, insbe sondere alkoholischem Alkali, behandelt.
<I>Beispiel</I> 15 Gewichtsteile Monobrom-Bzl, Bzl'- benzanthronylsulfid (erhalten durch Mono- bromieren von Bzl, Bzl'-benzanthronylsulfid in geeigneten Lösungsmitteln) werden bei 120' mit 90 Gewichtsteilen Atzkali und 75 Gewichtsteilen Äthylalkohol bis zur Be endigung der Reaktion verschmolzen. Die Schmelze wird mit Wasser .aufgenommen und Luft eingeleitet, solange noch Farbstoff in Form der Leukoverbindung vorhanden ist.
Man filtriert und wäscht gut mit. Wasser aus. Der erhaltene Farbstoff ist ein dunkel violettes Pülver, das sich in konzentrierter Schwefelsäure mit grüner Farbe löst und Baumwolle aus blauer Hydrosulfitküpe kräftig violett färbt. An Stelle von Äthylalkohol kann man auch andere Alkohole, an Stelle von Kali hydrat andere Ätzalkalien verwenden.
Method for the preparation of 1Ylonobromisoclibenzanthrone. The subject of this additional patent is a process for the preparation of monobromoisodibenzanthrone. The procedure consists in that one monobromo-Bzl, Bz1'-benzantlironylsulfid following gender formula:
EMI0001.0006
treated with alkaline condensation agents, in particular special alcoholic alkali.
<I> Example </I> 15 parts by weight of monobromo-Bzl, Bzl'-benzanthronyl sulfide (obtained by monobromination of Bzl, Bzl'-benzanthronyl sulfide in suitable solvents) are at 120 'with 90 parts by weight of caustic potash and 75 parts by weight of ethyl alcohol to Be termination of the reaction fused. The melt is absorbed with water and air is introduced as long as there is still dye in the form of the leuco compound.
It is filtered and washed well. Water out. The dye obtained is a dark purple powder that dissolves in concentrated sulfuric acid with a green color and gives cotton from a blue hydrosulfite vat a strong purple color. Instead of ethyl alcohol, other alcohols can be used, and other caustic alkalis can be used instead of potassium hydrate.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE120710X | 1924-10-20 | ||
CH119233T | 1927-12-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH120710A true CH120710A (en) | 1927-06-16 |
Family
ID=25709235
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH120710D CH120710A (en) | 1924-10-20 | 1925-10-19 | Process for the preparation of monobromoisodibenzanthrone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH120710A (en) |
-
1925
- 1925-10-19 CH CH120710D patent/CH120710A/en unknown
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