CH293003A - Process for the preparation of a nitro dye. - Google Patents
Process for the preparation of a nitro dye.Info
- Publication number
- CH293003A CH293003A CH293003DA CH293003A CH 293003 A CH293003 A CH 293003A CH 293003D A CH293003D A CH 293003DA CH 293003 A CH293003 A CH 293003A
- Authority
- CH
- Switzerland
- Prior art keywords
- nitro
- preparation
- nitro dye
- dye
- weight
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Nitrofarbstoffes. Gegenstand des vorliegenden Zusatzpaten tes ist ein Verfahren zur Herstellung eines Nitrofarbstoffes, welches dadurch gekenn zeichnet ist, dass man 1-Halogen-2-nitro-4- trifluormethylbenzol mit 4-Aminodiphenyl- äther-2-sulfonsäure kondensiert.
<I>Beispiel:</I> In einen Autoklaven werden 11 Gewichts teile Natriumcarbonat, 54 Gewiehtsteile 4- @lminodiphenyläther - 2 - sulfonsäure, 45 Ge wichtsteile 1-Chlor-2-nitro-4-trifluormethyl- ben7ol, 40 Gewichtsteile Schlämmkreide und \?00 Gewichtsteile Wasser verrührt. Dann wird mehrere Stunden bei einer Temperatur von l20 C weiter gerührt, bis die Umsetzung beendet ist.
Danach wird die verdünnte, seliwaeh alkaliseh gestellte Lösung geklärt und der Farbstoff ausgesalzen.
An Stelle von Wasser kann auch Alkohol verwendet werden. In gleicher Weise kann auch 1-Brom-2-nitro-4-trifluormethylbenzol eingesetzt werden.
Das so erhaltene Produkt stellt ein gelbes kristallines Pulver dar, das Wolle in rotstichig gelben Tönen von guten Echtheitseigenschaf ten, insbesondere von sehr guter Lichtechtheit, färbt.
Process for the preparation of a nitro dye. The subject of the present additional patent is a process for the production of a nitro dye, which is characterized in that 1-halo-2-nitro-4-trifluoromethylbenzene is condensed with 4-aminodiphenyl ether-2-sulfonic acid.
<I> Example: </I> In an autoclave are 11 parts by weight of sodium carbonate, 54 parts by weight of 4- @ lminodiphenyl ether - 2 - sulfonic acid, 45 parts by weight of 1-chloro-2-nitro-4-trifluoromethylben7ol, 40 parts by weight of chalk and \? 00 parts by weight of water stirred. Stirring is then continued for several hours at a temperature of 120 ° C. until the reaction has ended.
Then the diluted, seliwaeh alkaline solution is clarified and the dye is salted out.
Instead of water, alcohol can also be used. 1-Bromo-2-nitro-4-trifluoromethylbenzene can also be used in the same way.
The product thus obtained is a yellow crystalline powder which dyes wool in reddish yellow tones with good fastness properties, in particular very good lightfastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE293003X | 1949-11-07 | ||
CH289072T | 1950-10-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH293003A true CH293003A (en) | 1953-08-31 |
Family
ID=25732859
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH293003D CH293003A (en) | 1949-11-07 | 1950-10-17 | Process for the preparation of a nitro dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH293003A (en) |
-
1950
- 1950-10-17 CH CH293003D patent/CH293003A/en unknown
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