CH234965A - Process for the preparation of a polymethine dye. - Google Patents
Process for the preparation of a polymethine dye.Info
- Publication number
- CH234965A CH234965A CH234965DA CH234965A CH 234965 A CH234965 A CH 234965A CH 234965D A CH234965D A CH 234965DA CH 234965 A CH234965 A CH 234965A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- polymethine dye
- dye
- trifluoromethylsulfonylindoline
- trimethyl
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Herstellung eines Polymethinfarbstoffes. Gegenstand dieses Patentes ist ein Ver fahren zur Herstellung eines Polymethinfarb- stoffes, welches dadurch gekennzeichnet ist, dass man 1.3.3-Trimethyl-2-methylen-5-tri- fluormethylsulfonylindolin mit 4-(N-Äthyl- butyl)-amino-2-methyl-benzaldehyd konden siert.
<I>Beispiel:</I> 305 Gewichtsteile 1.3.3-Trimethyl-2-me- thylen-5-trifluormethylsulfonylindolin und 219 Gewichtsteile 4-(N-Äthyl-butyl)-amino- 2-methylbenzaldehyd werden in 900 Ge wichtsteilen Eisessig auf 70 bis 80 C erhitzt, bis die Farbstoffbildung beendet ist. Dann wird die Lösung des Farbstoffes in starke Salzsäurelösung gegeben und mit Natrium chlorid ausgesalzen. Der Farbstoff kristalli siert in bronzierenden Schuppen.
Er ist leicht in Wasser löslich und färbt Zelluloseester und -äther in einem rotstichigen Blau von guten Nassechtheiten und guter Lichtechtheit. Das angewandte Indolinderivat kann nach be kanntem Verfahren aus 4-Aminophenyltri- fluormethylsulfon hergestellt werden. Es ist ein ül vom gp, 176 bis 179 C, das sich schon nach kurzer Zeit rot färbt.
Process for the preparation of a polymethine dye. The subject of this patent is a process for the production of a polymethine dye, which is characterized in that 1,3.3-trimethyl-2-methylene-5-trifluoromethylsulfonylindoline with 4- (N-ethyl-butyl) -amino-2 -methyl-benzaldehyde condenses.
<I> Example: </I> 305 parts by weight of 1,3.3-trimethyl-2-methylene-5-trifluoromethylsulfonylindoline and 219 parts by weight of 4- (N-ethyl-butyl) -amino-2-methylbenzaldehyde in 900 parts by weight of glacial acetic acid heated to 70 to 80 C until dye formation has ended. Then the solution of the dye is poured into a strong hydrochloric acid solution and salted out with sodium chloride. The dye crystallizes in bronzing scales.
It is easily soluble in water and dyes cellulose esters and ethers in a reddish blue with good wet fastness and good light fastness. The indoline derivative used can be prepared from 4-aminophenyltrifluoromethylsulfone by known processes. It is a ül from gp, 176 to 179 C, which turns red after a short time.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE234965X | 1940-10-21 | ||
CH232375T | 1941-12-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH234965A true CH234965A (en) | 1944-10-31 |
Family
ID=25727710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH234965D CH234965A (en) | 1940-10-21 | 1941-12-02 | Process for the preparation of a polymethine dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH234965A (en) |
-
1941
- 1941-12-02 CH CH234965D patent/CH234965A/en unknown
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