CH120715A - Process for the preparation of Bz2-Bz2'-dimethoxyisodibenzanthrone. - Google Patents
Process for the preparation of Bz2-Bz2'-dimethoxyisodibenzanthrone.Info
- Publication number
- CH120715A CH120715A CH120715DA CH120715A CH 120715 A CH120715 A CH 120715A CH 120715D A CH120715D A CH 120715DA CH 120715 A CH120715 A CH 120715A
- Authority
- CH
- Switzerland
- Prior art keywords
- blue
- preparation
- dimethoxyisodibenzanthrone
- bzl
- dissolves
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung von Bz2-Bz2'-Diriiethogyisodibenzanthron. Das Verfahren besteht darin, dass man Bz2,Bz2'-Dimethogy-Bz1,Bz1'-benzanthronyl- sulfid von folgender I'ormel:
EMI0001.0008
mit alkalischen Kondensationsmitteln, insbe= sondere alkoholischem Alkali, behandelt.
Beispiel: 10 Gewichtsteile Bz2,Bz2'-Dimethpxy- Bz1,Bzl'-benzantUronylsulfid, erhalten durch Umsetzung von Bz2-Methoxy-Bzl-halogen- benzanthron mit Natriumpolysulfid werden in eine Schmelze von 50 Gewichtsteilen Ätz kali und-4 Gewichtsteilen Äthylalkohol bei ungefähr<B>130'</B> eingetragen und das Reak tionsgemisch bis zur Beendigung der Farb- stoffbildung bei dieser Tempeiatur gerührt.
Man verdünnt mit Wasser, leitet. in die Sus pension Luft ein, solange noch Farbstoff in Form der Leukoverbindung in. Lösung ist, filtriert und wäscht mit Wasser gut aus. Der.
Farbstoff stellt ein blauschwarzes Pulver dar; das sich in konzentrierter -Schwefelsäure mit rotvioletter Farbe löst und aus blauer Hydrosulfitküpe Baumwolle in blauen Tönen anf ärbt An Stelle von, Äthylalkohol kann man auch andere Alkohole, an Stelle von Kali hydrat andere Ätzälkalien verwenden.
Method for the preparation of Bz2-Bz2'-Diriiethogyisodibenzanthron. The procedure consists in that you get Bz2, Bz2'-Dimethogy-Bz1, Bz1'-benzanthronyl sulfide from the following formula:
EMI0001.0008
treated with alkaline condensation agents, especially alcoholic alkali.
Example: 10 parts by weight of Bz2, Bz2'-dimethpxy-Bz1, Bzl'-benzantUronylsulfid, obtained by reacting Bz2-methoxy-Bzl-halogen-benzanthrone with sodium polysulfide are in a melt of 50 parts by weight of caustic potash and -4 parts by weight of ethyl alcohol at about < B> 130 '</B> and the reaction mixture was stirred at this temperature until the formation of the dye had ended.
One dilutes with water, conducts. Air is introduced into the suspension as long as there is still dye in the form of the leuco compound in the solution, filtered and washed thoroughly with water. The.
Dye is a blue-black powder; which dissolves in concentrated sulfuric acid with a red-violet color and dyes cotton in blue tones from a blue hydrosulphite vat.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE120715X | 1924-10-20 | ||
CH119233T | 1927-12-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH120715A true CH120715A (en) | 1927-07-01 |
Family
ID=25709240
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH120715D CH120715A (en) | 1924-10-20 | 1925-10-19 | Process for the preparation of Bz2-Bz2'-dimethoxyisodibenzanthrone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH120715A (en) |
-
1925
- 1925-10-19 CH CH120715D patent/CH120715A/en unknown
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