CH124279A - Process for the production of a new dye. - Google Patents
Process for the production of a new dye.Info
- Publication number
- CH124279A CH124279A CH124279DA CH124279A CH 124279 A CH124279 A CH 124279A CH 124279D A CH124279D A CH 124279DA CH 124279 A CH124279 A CH 124279A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- phosgene
- aminonaphthol
- production
- dianotated
- 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
- C09B43/00—Preparation of azo dyes from other azo compounds
- C09B43/12—Preparation of azo dyes from other azo compounds by acylation of amino groups
- C09B43/136—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents
- C09B43/14—Preparation of azo dyes from other azo compounds by acylation of amino groups with polyfunctional acylating agents with phosgene or thiophosgene
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Farbstoffes. Es wurde gefunden, dass man einen neuen Azofarbstoff erhält, wenn man den Azofarb- stoff, welcher erhalten werden kann durch Vereinigen eines dianotierten und an der OH-Gruppe acidylierten Derivates der 1,8 Aminonaphthol-3,6-disulfosäure mit Kresidin (C113 :
OCHS : N112 =1: 4: 3), ein Verseif ungs- mittel, Phosgen und den Azofarbstoff, der er halten werden kann durch Vereinigen der dianotierten 2,5-Aminonaphthol-7-sulfosäure mit gresidin, <B>(0113:</B> OCHa : N112 =1: 4 : 3), auf einander einwirken lässt und so zu einem Harn stoffderivat verkettet. Der neue Farbstoff bildet ein braunrotes Pulver; er färbt ungebeizte Baumwolle in sehr egalen, orangeroten Tönen von sehr guter Lichtechtheit.
<I>Beispiel</I> 62,1 Teile des Farbstoffes aus dem diano tierten p-Toluolsulfosäureester der 1,8-Amino- naphthol-3,6-disulfosäure und Kresidin (0H3 OCHS :N112 = 1:4:3), sowie 38,7 Teile des Farbstoffes aus dianotierter 2,5-Aminonaphthol- 7-sulfosäure und gresidin (CHs : OCHS : N112 = 1 :4:
3) werden in sodaalkalischer Lösung bei 300 erschöpfend mit Phosgen behandelt und das erhaltene Harnstoffderivat. mit 3 % iger Natronlauge bei 900 verseift. Der neue Farb stoff wird in bekannter Weise isoliert.
Der gleiche Farbstoff entsteht auch, wenn man den Farbstoff aus dem Ester der 1,8- Aminonaphthol-3,6-disulfosäure zunächst; ver seift und dann mit dein zweiten Azokörper vereinigt.
Process for the production of a new dye. It has been found that a new azo dye is obtained if the azo dye, which can be obtained by combining a dianotated derivative of 1,8 aminonaphthol-3,6-disulfonic acid with cresidine (C113:
OCHS: N112 = 1: 4: 3), a saponifying agent, phosgene and the azo dye, which can be obtained by combining the dianotated 2,5-aminonaphthol-7-sulfonic acid with gresidin, <B> (0113: < / B> OCHa: N112 = 1: 4: 3), allowing them to act on each other and thus chaining them to a urea derivative. The new dye forms a brown-red powder; it dyes unstained cotton in very even, orange-red shades of very good lightfastness.
<I> Example </I> 62.1 parts of the dye from the diano-tated p-toluenesulfonic acid ester of 1,8-amino-naphthol-3,6-disulfonic acid and cresidine (0H3 OCHS: N112 = 1: 4: 3), and 38.7 parts of the dye from dianotated 2,5-aminonaphthol- 7-sulfonic acid and gresidin (CHs: OCHS: N112 = 1: 4:
3) are treated exhaustively with phosgene in a soda-alkaline solution at 300, and the urea derivative obtained. saponified with 3% sodium hydroxide solution at 900. The new dye is isolated in a known manner.
The same dye is also produced when the dye is first made from the ester of 1,8-aminonaphthol-3,6-disulfonic acid; soaped and then combined with your second azo body.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH124279T | 1926-07-10 | ||
CH123162T | 1926-07-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH124279A true CH124279A (en) | 1928-01-16 |
Family
ID=25710041
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH124279D CH124279A (en) | 1926-07-10 | 1926-07-10 | Process for the production of a new dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH124279A (en) |
-
1926
- 1926-07-10 CH CH124279D patent/CH124279A/en unknown
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