CH234963A - Process for the preparation of a polymethine dye. - Google Patents
Process for the preparation of a polymethine dye.Info
- Publication number
- CH234963A CH234963A CH234963DA CH234963A CH 234963 A CH234963 A CH 234963A CH 234963D A CH234963D A CH 234963DA CH 234963 A CH234963 A CH 234963A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- polymethine dye
- dye
- methylsulfonylindoline
- benzaldehyde
- Prior art date
Links
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- 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-me- thylsulfonylindolin mit 4 - (N - Methyl - 4' - äthoxyphenyl) - amino - benzaldehyd konden siert.
Beispiel: 251 Gewichtsteile 1.3.3-Trimethyl-2-me- thylen-5-methylsulfonylindolin und 255 Ge wichtsteile 4-(N-Methyl-4'-äthoxyphenyl)- amino-benzaldehyd werden in 600 Gewichts teilen Eisessig mehrere Stunden auf 70 bis 80 C erhitzt. Nach beendeter Farbstoffbil- dung wird die Lösung in starke Phosphor säure gegeben und mit saurem Natriumphos- phat ausgesalzen. Der Farbstoff kristalli siert in dunklen glänzenden Schuppen.
Er löst sich leicht in Wasser und färbt Zellu- loseester und -äther in violetten Tönen, die sich durch gute Lichtechtheit auszeichnen. Das als Ausgangsstoff verwendete Indo- linderivat kann aus p-Aminophenylmethyl- sulfon nach bekanntem Verfahren hergestellt werden. Es ist ein zähes<B>01</B> vom Kp."5 235 bis 237 C, das sich nach kurzer Zeit rötlich 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-methylsulfonylindoline with 4 - (N - methyl - 4 '- ethoxyphenyl) - Amino-benzaldehyde condenses.
Example: 251 parts by weight of 1,3.3-trimethyl-2-methylene-5-methylsulfonylindoline and 255 parts by weight of 4- (N-methyl-4'-ethoxyphenyl) -amino-benzaldehyde are in 600 parts by weight of glacial acetic acid to 70 to several hours 80 C heated. When the dye has formed, the solution is poured into strong phosphoric acid and salted out with acidic sodium phosphate. The dye crystallizes in dark, shiny scales.
It dissolves easily in water and colors cellulose esters and ethers in violet tones, which are characterized by good lightfastness. The indoline derivative used as the starting material can be prepared from p-aminophenylmethylsulfone by a known process. It is a tough <B> 01 </B> with bp "5 235 to 237 C, which turns reddish after a short time.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE234963X | 1940-10-21 | ||
CH232375T | 1941-12-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH234963A true CH234963A (en) | 1944-10-31 |
Family
ID=25727708
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH234963D CH234963A (en) | 1940-10-21 | 1941-12-02 | Process for the preparation of a polymethine dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH234963A (en) |
-
1941
- 1941-12-02 CH CH234963D patent/CH234963A/en unknown
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