CH301339A - Process for the preparation of a sulfonic acid amide of the anthraquinone series. - Google Patents
Process for the preparation of a sulfonic acid amide of the anthraquinone series.Info
- Publication number
- CH301339A CH301339A CH301339DA CH301339A CH 301339 A CH301339 A CH 301339A CH 301339D A CH301339D A CH 301339DA CH 301339 A CH301339 A CH 301339A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid amide
- sulfonic acid
- preparation
- anthraquinone series
- anthraquinone
- 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
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
- C09B1/26—Dyes with amino groups substituted by hydrocarbon radicals
- C09B1/32—Dyes with amino groups substituted by hydrocarbon radicals substituted by aryl groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Description
Zusatzpatent zum Hauptpatent Nr. <B>297845.</B> Verfahren zur Herstellung eines Sulfonsäureamides der Anthrachinonreihe. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines SuHon- säureamides der Anthraehinonreihe, welches darin besteht, dass man<B>1</B> Mol des nach der Schweizer Patentschrift Nr.295891 erhältli- ehen 1,4-Di-(2',6-dimethyl)
-phenyla#mino- anthraehinondisulionsäurechlorides mit 2 Mol Aminomethan kondensiert.
Im nachfolgenden Beispiel bedeuten die Teile Gewichtsteile.
<I>Beispiel:</I> Man verrührt das nach den Angaben der Schweizer Patentsc#I-1rift Nr. <B>295891</B> aus 44,6 Teilen 1,4-Di-(2',6-dimethyl)-phenylamino- anthraehinon erhältliche Disulfonsäurechlorid in Form einer wässerigen, neutralen Paste bei <B><U>900</U></B> mit 200 Teilen Wasser und<B>65</B> Teilen 350./oi-er Aminomethanlösung. Hierauf erhöht <B>kn</B> man die Temperatur des Gemisches innert einer Stunde auf 450 und rührt es bei dieser Temperatur bis zur vollständigen Umsetzung weiter, was etwa<B>5</B> Stunden beansprucht.
Das Kondensationsprodukt isoliert man aus der wässerigen Suspension durch Filtrieren, be- f reit es von der Mutterlauge durch Auswaschen mit kaltem Wasser und trocknet es bei 800.
Das neue Sulionsäureamid der Anthrachi- nonreihe ist ein rotstiehig blaues, in Wasser unlösliches Pulver. Es löst sich mit blauer Farbe in kalter<B>1</B> 1/o iger Natriumliydroxyd- lösung, in konzentrierter Schwefelsäure, in (-r'lyeolmonoäthyläther und in Cyclohexanol. Es dient zum Färben von Lacken und plasti- sehen Massen.
Additional patent to main patent no. <B> 297845. </B> Process for the production of a sulfonic acid amide of the anthraquinone series. The subject of the present patent is a process for the preparation of a SuHonic acid amide of the anthraehinone series, which consists in that <B> 1 </B> mol of the 1,4-di- (2 ', 6-dimethyl)
-phenyla #mino- anthraehinondisulionsäurechlorides condensed with 2 mol of aminomethane.
In the following example, the parts are parts by weight.
<I> Example: </I> The mixture is stirred in accordance with the information in Swiss Patentsc # I-1rift No. <B> 295891 </B> from 44.6 parts of 1,4-di- (2 ', 6-dimethyl ) -phenylamino-anthraehinone available disulfonic acid chloride in the form of an aqueous, neutral paste at <B><U>900</U> </B> with 200 parts of water and <B> 65 </B> parts of 350./oi-er Aminomethane solution. The temperature of the mixture is then increased to 450 within an hour and it is stirred at this temperature until the reaction is complete, which takes about 5 hours.
The condensation product is isolated from the aqueous suspension by filtration, it is freed from the mother liquor by washing with cold water and it is dried at 800 m.
The new sulionic acid amide of the anthraquinone series is a reddish blue powder that is insoluble in water. It dissolves with a blue color in cold <B> 1 </B> 1 / o sodium hydroxide solution, in concentrated sulfuric acid, in -r'lyeol monoethyl ether and in cyclohexanol. It is used to color paints and plastic materials.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH297845T | 1951-10-18 | ||
CH301339T | 1951-10-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH301339A true CH301339A (en) | 1954-08-31 |
Family
ID=25733895
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH301339D CH301339A (en) | 1951-10-18 | 1951-10-18 | Process for the preparation of a sulfonic acid amide of the anthraquinone series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH301339A (en) |
-
1951
- 1951-10-18 CH CH301339D patent/CH301339A/en unknown
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