CH197476A - Process for the preparation of a polymethine dye. - Google Patents
Process for the preparation of a polymethine dye.Info
- Publication number
- CH197476A CH197476A CH197476DA CH197476A CH 197476 A CH197476 A CH 197476A CH 197476D A CH197476D A CH 197476DA CH 197476 A CH197476 A CH 197476A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- polymethine dye
- dye
- new
- formyl
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Indole Compounds (AREA)
Description
Verfahren zur Herstellung eines Polymethinfarbstof%s. Im Hauptpatent ist ein Verfahren zur Her stellung eines neuen Polymethinfarbstoffes beschrieben, bei dem man N-Formyl-2,3-di- hydro-a-methylindol in Gegenwart eines chlor haltigen Kondensationsmittels, wie Phosphor- oxychlorid oder Phosgen, gegebenenfalls in einem Lösungsmittel, mit 1,3,3-Trimethyl-2- methylenindolin in etwa molekularen Mengen umsetzt.
Es wurde nun gefunden, dass man eben falls einen neuen, wertvollen Polymethinfarb- atoff erhält, wenn man unter den oben ge schilderten Bedingungen N-Formyl-1,2,3,4- tetrahydrochinolin mit 1,3,3-Trimethyl-2-me- thylenindolin umsetzt.
Der Farbstoff zeichnet sich durch hervor ragende Klarheit und sehr gute Lichtechtheit aus.
<I>Beispiel:</I> Man versetzt eine Lösung von 35 Teilen N-Formyl-1,2,3,4-tetrahydrochinolin in 45 Tei len Benzol unterhalb 10<B>0 0</B> mit 32 Teilen Phosphoroxycblorid und tropft bei 0-5 C 34 Teile 1,3,3-Trimethyl-2-methylenindolin in diese Lösung. Beim Aufarbeiten in der im Beispiel der Hauptanmeldung beschriebenen Weise erhält man gelbe Kristalle, die auf tannierter Baumwolle klare, grüngelbe Fär bungen liefern.
Method of making a polymethine dye% s. The main patent describes a process for preparing a new polymethine dye, in which N-formyl-2,3-dihydro-a-methylindole is used in the presence of a chlorine-containing condensing agent such as phosphorus oxychloride or phosgene, optionally in a solvent with 1,3,3-trimethyl-2-methyleneindoline in approximately molecular amounts.
It has now been found that a new, valuable polymethine dye is also obtained if N-formyl-1,2,3,4-tetrahydroquinoline is combined with 1,3,3-trimethyl-2- under the conditions described above. methylene indoline converts.
The dye is characterized by excellent clarity and very good lightfastness.
<I> Example: </I> A solution of 35 parts of N-formyl-1,2,3,4-tetrahydroquinoline in 45 parts of benzene below 10 0 0 is mixed with 32 parts of phosphorus oxychloride and 34 parts of 1,3,3-trimethyl-2-methyleneindoline are added dropwise to this solution at 0-5 C. When working up in the manner described in the example of the main application, yellow crystals are obtained which give clear, greenish-yellow colorations on tannic cotton.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE197476X | 1935-08-16 | ||
CH193624T | 1936-07-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH197476A true CH197476A (en) | 1938-04-30 |
Family
ID=25722550
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH197476D CH197476A (en) | 1935-08-16 | 1936-07-02 | Process for the preparation of a polymethine dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH197476A (en) |
-
1936
- 1936-07-02 CH CH197476D patent/CH197476A/en unknown
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