CH175902A - Process for the preparation of an acidic triphenylmethane dye. - Google Patents
Process for the preparation of an acidic triphenylmethane dye.Info
- Publication number
- CH175902A CH175902A CH175902DA CH175902A CH 175902 A CH175902 A CH 175902A CH 175902D A CH175902D A CH 175902DA CH 175902 A CH175902 A CH 175902A
- Authority
- CH
- Switzerland
- Prior art keywords
- acidic
- preparation
- triphenylmethane dye
- effected
- way
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines sauren Triphenylmethanfarbstoffes. Gegenstand des vorliegenden Zusatzpa tentes ist ein Verfahren zur Darstellung eines sauren Triphenylmethanfarbstoffes, wel ches darin besteht, dass man 4,4'-Dichlor- benzophenon mit symmetrischen Di-n-butyl- m-xylidin kondensiert, dann das so erhaltene Kondensationsprodukt mit p-Aminodiphenyl- äther umsetzt,
wodurch die in 4- und 4'- Stellung befindlichen Chloratome durch die Basenreste ersetzt werden, und die so erhal tene Verbindung sulfiert.
<I>Beispiel:</I> 25 Gewichtsteile 4,4'-Dichlorbenzophenon werden mit<B>23,5</B> Gewichtsteilen symmetri schem Di-n-butyl-m-xylidin in Gegenwart von 20 Gewichtsteilen Phosphoroxychlorid durch mehrstündiges Kochen in 100 Gewichts teilen Toluol kondensiert. Nach Abdestillie- ren des Toluols und des noch vorhandenen Phosphoroxychlorids wird das Kondensations produkt mit 60 Gewichtsteilen p-Aminodi- phenyläther verschmolzen.
Der überschüssige p-Aminodiphenyläther wird nach dem Erkal ten der Schmelze durch Ausrühren mit ver dünnter Salzsäure entfernt. Der so entstan dene wasserunlösliche blaue Farbstoff wird isoliert und auf bekannte Weise sulfiert. Die so erhältliche Farbstoffdisulfosäure färbt als Natriumsalz Wolle und Seide in leuchtend sehr grünstichig-blauen Tönen von sehr gu ter Lichtechtheit und vorzüglicher Abendfarbe.
Process for the preparation of an acidic triphenylmethane dye. The subject of the present additional patent is a process for the preparation of an acidic triphenylmethane dye which consists in condensing 4,4'-dichlorobenzophenone with symmetrical di-n-butyl- m-xylidine, then the condensation product thus obtained with Aminodiphenyl ether converts,
whereby the chlorine atoms in the 4- and 4'-positions are replaced by the base radicals, and the compound thus obtained is sulfated.
<I> Example: </I> 25 parts by weight of 4,4'-dichlorobenzophenone are mixed with <B> 23.5 </B> parts by weight of symmetrical di-n-butyl-m-xylidine in the presence of 20 parts by weight of phosphorus oxychloride by boiling for several hours condensed in 100 parts by weight of toluene. After the toluene and the phosphorus oxychloride still present have been distilled off, the condensation product is fused with 60 parts by weight of p-aminodiphenyl ether.
The excess p-aminodiphenyl ether is removed after the melt has cooled by stirring with dilute hydrochloric acid. The resulting water-insoluble blue dye is isolated and sulfated in a known manner. The sodium salt of the dye disulfonic acid obtainable in this way dyes wool and silk in bright, very greenish-blue shades of very good lightfastness and an excellent evening color.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE175902X | 1933-06-15 | ||
CH170094T | 1933-08-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH175902A true CH175902A (en) | 1935-03-15 |
Family
ID=25718877
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH175902D CH175902A (en) | 1933-06-15 | 1934-06-13 | Process for the preparation of an acidic triphenylmethane dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH175902A (en) |
-
1934
- 1934-06-13 CH CH175902D patent/CH175902A/en unknown
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