CH167402A - Process for the preparation of a dye. - Google Patents
Process for the preparation of a dye.Info
- Publication number
- CH167402A CH167402A CH167402DA CH167402A CH 167402 A CH167402 A CH 167402A CH 167402D A CH167402D A CH 167402DA CH 167402 A CH167402 A CH 167402A
- Authority
- CH
- Switzerland
- Prior art keywords
- dye
- weight
- parts
- amino
- preparation
- Prior art date
Links
Landscapes
- Coloring (AREA)
Description
Verfahren zur Darstellung eines Farbstoffes. Gegenstand vorliegenden Patentes ist ein Verfahren zur Darstellung eines Farb stoffes, welches dadurch gekennzeichnet ist. dass man 2 . 5 - Di - (N - acetylcarbazoyl - 3'- amino)-3.6-dichlor-1.4-benzochinon in einem hochsiedenden Lösungsmittel erhitzt.
<I>Beispiele:</I> 1. 200 Gewichtsteile 2.5-Di-(N-acetyl- car bazoyl-3'-amino)-3 . 6-dichlor-1 . 4-benzo- chinon werden in 3000 Gewichtsteilen Nitro- benzol 6 Stunden zum Sieden erhitzt. Das Kondensationsprodukt wird nach dem Erkal ten abgesaugt, mit Nitrobenzol und Alkohol gewaschen und getrocknet. Es ist ein grau grüner Stoff, der sich in konzentrierter Schwefelsäure mit blauer Farbe löst; sulfiert färbt es Baumwolle in lichtechten blauviolet ten Tönen an.
Das 2. 5-Di-(N-acetylcarbazoyl-3'-amino)- 3.6-dichlor-1.4-benzochinon wird durch Kondensation von Chloranil und 3-Amido- N-acetylcarbazol erhalten; es ist ein rötlich brauner Stoff, der sich violett in konzen trierter Schwefelsäure löst. Das 3-Amino-N- acetylcarbazol bildet sich bei der Reduktion der entsprechenden Nitroverbindung.
2. Eine Mischung von 1000 Gewichtstei len Trichlorbenzol, 45 Gewichtsteilen 3 Amino-N-acetyl-carbazol, 25 Gewichtsteilen 2.3.5.6-Tetrachlor-1 .4-benzochinon und von 17 Gewichtsteilen wasserfreiem Natrium acetat werden nach Zugabe von 50 Gewichts teilen 2 . 4-Dinitrophenol auf 200 bis 210 C geheizt und 6 Stunden bei dieser Temperatur nachgerührt. Nach dem Erkalten wird das ausgeschiedene Kondensationsprodukt abge saugt und mit Nitrobenzol, Alkohol und Wasser gewaschen. Er ist mit dem nach Beispiel 1 erhaltenen Farbstoff identisch.
Process for the preparation of a dye. The subject of the present patent is a method for displaying a dye, which is characterized. that one 2. 5 - Di - (N - acetylcarbazoyl - 3'-amino) -3.6-dichloro-1,4-benzoquinone heated in a high-boiling solvent.
<I> Examples: </I> 1. 200 parts by weight of 2.5-di- (N-acetylcarbazoyl-3'-amino) -3. 6-dichloro-1. 4-benzoquinone are heated to boiling in 3000 parts by weight of nitrobenzene for 6 hours. After cooling, the condensation product is filtered off with suction, washed with nitrobenzene and alcohol and dried. It is a gray-green substance that dissolves in concentrated sulfuric acid with a blue color; sulfated, it stains cotton in lightfast blue-violet tones.
The 2. 5-di- (N-acetylcarbazoyl-3'-amino) -3,6-dichloro-1,4-benzoquinone is obtained by condensation of chloranil and 3-amido-N-acetylcarbazole; it is a reddish brown substance that dissolves in purple in concentrated sulfuric acid. The 3-amino-N-acetylcarbazole is formed when the corresponding nitro compound is reduced.
2. A mixture of 1000 parts by weight of trichlorobenzene, 45 parts by weight of 3 amino-N-acetyl-carbazole, 25 parts by weight of 2.3.5.6-tetrachloro-1 .4-benzoquinone and 17 parts by weight of anhydrous sodium acetate are added after adding 50 parts by weight 2. 4-Dinitrophenol heated to 200 to 210 C and stirred for 6 hours at this temperature. After cooling, the precipitated condensation product is filtered off with suction and washed with nitrobenzene, alcohol and water. It is identical to the dye obtained in Example 1.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH148120T | 1929-05-30 | ||
DE167402X | 1932-01-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH167402A true CH167402A (en) | 1934-02-15 |
Family
ID=25715153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH167402D CH167402A (en) | 1929-05-30 | 1933-01-26 | Process for the preparation of a dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH167402A (en) |
-
1933
- 1933-01-26 CH CH167402D patent/CH167402A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH167402A (en) | Process for the preparation of a dye. | |
US1904367A (en) | 7.7'-dichloro flavanthrone and the process of making same | |
DE546228C (en) | Process for the production of nitrogen-containing Kuepen dyes | |
CH167403A (en) | Process for the preparation of a dye. | |
DE386056C (en) | Process for the production of Kuepen dyes | |
CH149614A (en) | Process for the preparation of a vat dye. | |
DE518951C (en) | Process for the preparation of purple indigoid dyes | |
CH167401A (en) | Process for the preparation of a dye. | |
CH188225A (en) | Process for the production of a vat dye of the anthraquinone series. | |
CH292691A (en) | Process for the production of a vat dye. | |
CH265735A (en) | Process for the production of a vat dye. | |
CH272571A (en) | Process for the production of a vat dye. | |
CH222472A (en) | Process for the production of a nitrogen-containing condensation product. | |
CH146858A (en) | Process for the preparation of a vat dye of the benzanthrone pyrazole anthrone series. | |
CH292689A (en) | Process for the production of a vat dye. | |
CH224887A (en) | Process for the production of a vat dye. | |
CH224886A (en) | Process for the production of a vat dye. | |
CH188224A (en) | Process for the preparation of an oxazole dye of the anthraquinone series. | |
CH103888A (en) | Process for the preparation of a condensation product of the benzanthrone series. | |
CH350056A (en) | Process for the production of vat dyes of the acedianthron series | |
CH265734A (en) | Process for the production of a vat dye. | |
CH150190A (en) | Process for the preparation of a vat dye of the benzanthrone pyrazole anthrone series. | |
CH247611A (en) | Process for the production of a vat dye. | |
CH265733A (en) | Process for the production of a vat dye. | |
CH145886A (en) | Process for the production of an anthraquinone derivative. |