CH120709A - Process for the preparation of dichloroisodibenzanthrone. - Google Patents
Process for the preparation of dichloroisodibenzanthrone.Info
- Publication number
- CH120709A CH120709A CH120709DA CH120709A CH 120709 A CH120709 A CH 120709A CH 120709D A CH120709D A CH 120709DA CH 120709 A CH120709 A CH 120709A
- Authority
- CH
- Switzerland
- Prior art keywords
- bzl
- dichloroisodibenzanthrone
- preparation
- benzanthronyl
- sulfide
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von Dichlorisodibenzanthron. Gegenstand dieses Zusatzpatentes ist ein Verfahren zur" Darstellung von Dichlor- isodibenzanthron. Das Verfahren besteht darin,. dass man Dichlor-Bzl, Bzl'-benzanthrony1sulfid fol gender -Formel:
EMI0001.0006
mit alkalischen Kondensationsmitteln, insbe sondere alkoholischem. Alkali, behandelt.
<I>Beispiel</I> 10 Gewichtsteile Dichlor-Bzl, Bzl'-benz- anthronylsulfid, erhalten beispielsweise durch Behandeln von Bzl, Bzl' - Benzanthronyl- sulfid mit der entsprechenden Menge Sul- furylchlorid im organischen Lösungsmittel oder -durch Umsetzung von Dichlorbenzan- thron mit Alkalipolysulfid,
werden bei 110 bis 120 in eine aus 60 Gewichtsteilen Ätz kali und 50 Gewichtsteilen Äthylalkohol hergestellte Schmelze eingetragen. Man hält das Reaktionsgemisch eine halbe bis eine Stunde bei dieser Temperatur,, nimmt mit Wasser auf,. leitet in die Suspension Luft, bis kein Farbstoff mehr als Leukoverbin- dung vorhanden ist, filtriert und wäscht mit Wasser.
Der erhaltene Farbstoff stellt ein dunkelviolettes Pulver dar, das. sich in Schwefelsäure mit grüner Farbe löst und aus .blauer Hydrosulfitküpe Baumwolle in kräftig violettem Tönen von vorzüglichen Echtheitseigenschaften anfärbt.
An Stelle von Äthylalkohol kann man auch andere Alkohole, an Stelle von Kali hydrat andere Ätzalkalien verwenden.
Process for the preparation of dichloroisodibenzanthrone. The subject of this additional patent is a process for the "preparation of dichloroisodibenzanthrone. The process consists in that dichloro-Bzl, Bzl'-benzanthrony1sulfide following gender formula:
EMI0001.0006
with alkaline condensation agents, especially alcoholic. Alkali, treated.
<I> Example </I> 10 parts by weight of dichloro-Bzl, Bzl'-benzanthronyl sulfide, obtained, for example, by treating Bzl, Bzl'-benzanthronyl sulfide with the corresponding amount of sulfuryl chloride in an organic solvent or by reacting dichlorobenzane - throne with alkali polysulphide,
are entered at 110 to 120 in a melt produced from 60 parts by weight of caustic potash and 50 parts by weight of ethyl alcohol. The reaction mixture is kept at this temperature for half an hour to an hour, taken up with water. passes air into the suspension until there is no more dye present as a leuco compound, filtered and washed with water.
The dye obtained is a dark violet powder which dissolves in sulfuric acid with a green color and, from a blue hydrosulfite vat, dyes cotton in strong violet tones with excellent fastness properties.
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 |
---|---|---|---|
DE120709X | 1924-10-20 | ||
CH119233T | 1927-12-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH120709A true CH120709A (en) | 1927-06-16 |
Family
ID=25709234
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH120709D CH120709A (en) | 1924-10-20 | 1925-10-19 | Process for the preparation of dichloroisodibenzanthrone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH120709A (en) |
-
1925
- 1925-10-19 CH CH120709D patent/CH120709A/en unknown
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