CH190904A - Process for the preparation of an indigoid dye of the pyrene series. - Google Patents
Process for the preparation of an indigoid dye of the pyrene series.Info
- Publication number
- CH190904A CH190904A CH190904DA CH190904A CH 190904 A CH190904 A CH 190904A CH 190904D A CH190904D A CH 190904DA CH 190904 A CH190904 A CH 190904A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- pyrene
- indigoid dye
- bordo
- series
- Prior art date
Links
Landscapes
- Coloring (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines indigoiden Farbstoffes der Pyrenreihe. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Darstellung eines indigoi- den Farbstoffes der Pyrenreihe, welches da durch gekennzeichnet ist, dass man 4,3-Pyren- 3'-ogythiophen mit Acenaphthenchinon kon densiert.
<I>Beispiel:</I> 27,4 Gewichtsteile 4,3-Pyren-3'-ogythio- phen werden in 3000 Gewichtsteilen Eisessig, und 19,1 Gewichtsteile Acenaphthenchinon werden in 1000 Gewichtsteilen Eisessig heiss gelöst. Die beiden Lösungen werden heiss zusammengegeben, mit einer kleinen Menge konzentrierter Salzsäure versetzt und einige Zeit gekocht. Dann wird heiss abgenutscht und zuerst mit heissem Eisessig, dann mit Alkohol gewaschen. Der rotbraune Farbstoff lässt sich z.
B. aus Trichlorbenzol umkristalli- sieren und färbt, aus konzentrierter Schwefel säure umgelöst, aus bordogefärbter Hydro- sulfitküpe ein kräftiges Bordo.
Process for the preparation of an indigoid dye of the pyrene series. The subject of the present patent is a process for the preparation of an indigoid dye of the pyrene series, which is characterized by the fact that 4,3-pyrene-3'-ogythiophene is condensed with acenaphthenequinone.
<I> Example: </I> 27.4 parts by weight of 4,3-pyrene-3'-ogythiophene are dissolved in 3000 parts by weight of glacial acetic acid, and 19.1 parts by weight of acenaphthenquinone are dissolved in 1000 parts by weight of hot glacial acetic acid. The two solutions are combined while hot, mixed with a small amount of concentrated hydrochloric acid and boiled for a while. Then it is sucked off hot and washed first with hot glacial acetic acid, then with alcohol. The red-brown dye can be z.
B. recrystallize from trichlorobenzene and color, redissolved from concentrated sulfuric acid, from a bordo-colored hydrosulfite vat a strong bordo.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE190904X | 1934-07-18 | ||
CH186852T | 1935-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH190904A true CH190904A (en) | 1937-05-15 |
Family
ID=25721458
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH190904D CH190904A (en) | 1934-07-18 | 1935-07-17 | Process for the preparation of an indigoid dye of the pyrene series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH190904A (en) |
-
1935
- 1935-07-17 CH CH190904D patent/CH190904A/en unknown
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