DE479027C - Process for the preparation of brown Kuepen colors - Google Patents
Process for the preparation of brown Kuepen colorsInfo
- Publication number
- DE479027C DE479027C DEI31129D DEI0031129D DE479027C DE 479027 C DE479027 C DE 479027C DE I31129 D DEI31129 D DE I31129D DE I0031129 D DEI0031129 D DE I0031129D DE 479027 C DE479027 C DE 479027C
- Authority
- DE
- Germany
- Prior art keywords
- brown
- preparation
- kuepen
- colors
- dye
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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
- C09B3/00—Dyes with an anthracene nucleus condensed with one or more carbocyclic rings
- C09B3/02—Benzathrones
- C09B3/06—Preparation from starting materials already containing the benzanthrone nucleus
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Coloring (AREA)
Description
Verfahren zur Darstellung brauner Küpeniarbstoffe In dem Hauptpatent 478 o47 ist ein Verfahren zur Darstellung eines braunen Küpenfarbstoffes beschrieben, bei dem der gemäß Beispiel i des Patents 475 342 durch Reduktion des nach dem französischen Patent 349531, Zusatz 6435, Beispie12 gewonnenenNitrobenzanthrons undVerschmelzen mit alkoholischem Kali erhältliche grüne Küpenfarbstoff mit oxydierenden Mitteln behandelt wird.Process for the preparation of brown vat dye In the main patent 478 047 a process for the preparation of a brown vat dye is described in which the green one obtained according to example i of patent 475 342 by reducing the nitrobenzanthrone obtained according to French patent 349531, addition 6435, example 12 and melting it with alcoholic potash Vat dye is treated with oxidizing agents.
Es hat sich nun gezeigt, daß man braune Küpenfarbstoffe ähnlicher Art auf einfache Weise auch darstellen kann, wenn man das vorerwähnte Nitrobenzanthron direkt mit alkalischen Mitteln behandelt. Die erhaltenen Farbstoffe können durch Behandeln mit Oxydationsmitteln, wie Hypochlorit, gereinigt werden. Beispiel :io Teile des nach dem französischen Patent 349 531, Zusatz 6435, Beispiel 2 erhältlichen Nitrobenzanthrons werden bei i2o' in eine Schmelze von alkoholischem Kali, die durch Erwärmen von 50 Teilen Kaliumhydroxyd mit 5o Teilen Äthylalkohol hergestellt wurde, eingetragen. Man hält die Temperatur 1/9 Stunde bei j:2o', erwärmt darauf langsam unter Abdestillieren des Alkohols auf 140 ' und hält die Schmelze bei dieser Temperatur, bis die Farbstoffbildung beendet ist. Nach dem Erkalten wird die Schmelze in Wasser gegeben, ausgeblasen und der Farbstoff abgesaugt und getrocknet. Der so erhaltene Farbstoff löst sich in konzentrierter Schwefe Isäure rotviolett und färbt Baumwolle aus blauer Küpe in echten braunen Tönen. Einen Farbstoff von reinerer Nuance erhält man, wenn man den rohen Farbstoff noch mit Hypochlorit aufkocht. Die Ausfärbung dieses Produktes geht beim Chlorieren auf der Faser in ein rötliches Orange Über.It has now been shown that brown vat dyes of a similar type can also be produced in a simple manner if the aforementioned nitrobenzanthrone is treated directly with alkaline agents. The dyes obtained can be purified by treatment with oxidizing agents such as hypochlorite. Example: 10 parts of the nitrobenzanthrone obtainable according to French patent 349 531, addendum 6435, example 2 are entered at 10 'in a melt of alcoholic potash, which was prepared by heating 50 parts of potassium hydroxide with 50 parts of ethyl alcohol. The temperature is maintained for 1/9 hour at j: 20 ', then slowly heated to 140 ' while distilling off the alcohol and the melt is kept at this temperature until the formation of the dye has ended. After cooling, the melt is poured into water, blown out and the dye is suctioned off and dried. The dye thus obtained dissolves in concentrated sulfuric acid red-violet and dyes cotton from a blue vat in real brown shades. A dye with a purer shade can be obtained if the raw dye is boiled with hypochlorite. The color of this product changes to a reddish orange on the fiber when chlorinated.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI31129D DE479027C (en) | 1927-05-11 | 1927-05-11 | Process for the preparation of brown Kuepen colors |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEI31129D DE479027C (en) | 1927-05-11 | 1927-05-11 | Process for the preparation of brown Kuepen colors |
Publications (1)
Publication Number | Publication Date |
---|---|
DE479027C true DE479027C (en) | 1929-07-09 |
Family
ID=7187796
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEI31129D Expired DE479027C (en) | 1927-05-11 | 1927-05-11 | Process for the preparation of brown Kuepen colors |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE479027C (en) |
-
1927
- 1927-05-11 DE DEI31129D patent/DE479027C/en not_active Expired
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE479027C (en) | Process for the preparation of brown Kuepen colors | |
DE536294C (en) | Process for the preparation of Kuepen dyes of the anthraquinone series | |
DE582613C (en) | Process for the production of asymmetrical indigoid dyes | |
DE469343C (en) | Process for the preparation of indigoid dyes | |
DE568036C (en) | Process for the production of indigoid dyes from alkyloxy-2íñ1-naphthisatines | |
DE515680C (en) | Process for the preparation of pyrazolanthrone-2-carboxylic acid | |
DE475342C (en) | Process for the preparation of Kuepen dyes | |
DE524362C (en) | Process for the production of Kuepen dyes | |
DE469249C (en) | Process for the production of indigoid dyes | |
DE497825C (en) | Process for the preparation of nitrogenous cow dyes | |
DE526973C (en) | Process for the preparation of Kuepen dyes | |
DE432579C (en) | Process for the production of Kuepen dyes of the anthraquinone series | |
DE396111C (en) | Process for the preparation of chlorine-free derivatives of N-dihydroanthraquinone azine | |
DE535069C (en) | Process for the preparation of 6-nitroacenaphthen-5-carboxylic acid | |
DE498066C (en) | Process for the preparation of Kuepen dyes | |
CH139393A (en) | Process for the preparation of a vat dye. | |
CH181719A (en) | Process for the production of a new dye of the anthraquinone series. | |
CH151965A (en) | Process for the production of a sulfur dye. | |
CH139390A (en) | Process for the preparation of a vat dye. | |
CH141317A (en) | Process for the preparation of a brown vat dye. | |
CH184190A (en) | Process for the production of a vat dye. | |
CH154048A (en) | Process for the production of a new chlorine-containing dye of the dibenzanthrone series. | |
CH148986A (en) | Process for the preparation of a vat dye. | |
CH148373A (en) | Process for the preparation of a vat dye. | |
CH109647A (en) | Process for the production of a new vat dye. |