CH190042A - Process for the preparation of a nitro dye. - Google Patents
Process for the preparation of a nitro dye.Info
- Publication number
- CH190042A CH190042A CH190042DA CH190042A CH 190042 A CH190042 A CH 190042A CH 190042D A CH190042D A CH 190042DA CH 190042 A CH190042 A CH 190042A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- nitro dye
- dye
- good fastness
- weight
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Nitrofarbstoffes. Gegenstand des vorliegenden Zusatzpaten tes ist ein Verfahren zur Darstellung eines Nitrofarbstoffes, welches dadurch gekenn zeichnet ist, dass man 1-Chlor-2-nitrobenzol- 4-sulfanilid mit 4-Aminodiphenylamin-2-sul- fonsäure kondensiert.
<I>Beispiel:</I> 264 Gewichtsteile 4-Aminodiphenylamin- 2-sulfonsäure werden durch Eintragen in eine Lösung von 53 Gewichtsteilen Natriumcar- bonat in der 1.5fachen Menge Wasser bei <B>6,0'</B> C in das Natriumsalz übergeführt. Nach Zugabe von 20 Gewichtsteilen Magnesium ogyd und 313 Gewichtsteilen 1-Chlor-2-nitro- benzol-4-sulfa.nilid wird 15 Stunden am Rückfluss zum Sieden erhitzt, bis keine dia- zotierbare Base mehr nachweisbar ist.
Dann wird durch Zugabe von 53 Gewichtsteilen Natriumcarbonat der Nitrofarbstoff in das Natriumsalz übergeführt, filtriert und mit Chlornatrium ausgefällt.
Er bildet in getrocknetem Zustand ein dunkelbraunes Pulver, das Wolle, Seide und Leder in gelbbraunen Tönen von guten Echt heitseigenschaften, insbesondere sehr guter Waschechtheit und Lichtechtheit färbt.
Process for the preparation of a nitro dye. The subject of the present additional patent is a process for the preparation of a nitro dye, which is characterized in that 1-chloro-2-nitrobenzene-4-sulfanilide is condensed with 4-aminodiphenylamine-2-sulfonic acid.
<I> Example: </I> 264 parts by weight of 4-aminodiphenylamine-2-sulfonic acid are added to a solution of 53 parts by weight of sodium carbonate in 1.5 times the amount of water at <B> 6.0 '</B> C in transferred to the sodium salt. After the addition of 20 parts by weight of magnesium oxide and 313 parts by weight of 1-chloro-2-nitrobenzene-4-sulfa.nilide, the mixture is refluxed for 15 hours until no more diazotizable base can be detected.
Then, by adding 53 parts by weight of sodium carbonate, the nitro dye is converted into the sodium salt, filtered and precipitated with sodium chloride.
In the dried state, it forms a dark brown powder which colors wool, silk and leather in yellow-brown shades of good fastness properties, in particular very good fastness to washing and light fastness.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE190042X | 1934-12-22 | ||
CH187696T | 1935-12-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH190042A true CH190042A (en) | 1937-03-31 |
Family
ID=25721572
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH190042D CH190042A (en) | 1934-12-22 | 1935-12-18 | Process for the preparation of a nitro dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH190042A (en) |
-
1935
- 1935-12-18 CH CH190042D patent/CH190042A/en unknown
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