CH122932A - Process for the preparation of a vat dye of the thioindigo series. - Google Patents
Process for the preparation of a vat dye of the thioindigo series.Info
- Publication number
- CH122932A CH122932A CH122932DA CH122932A CH 122932 A CH122932 A CH 122932A CH 122932D A CH122932D A CH 122932DA CH 122932 A CH122932 A CH 122932A
- Authority
- CH
- Switzerland
- Prior art keywords
- dimethylthioindigo
- dichloro
- preparation
- vat dye
- thioindigo series
- Prior art date
Links
Landscapes
- Indole Compounds (AREA)
- Lasers (AREA)
Description
Verfahren zur Herstellung eines Küpenfarbstoffes der Thioindigoreihe. Es wurde gefunden, dass man einen neuen Küpenfarbstoff der Thioindigoreihe erhält, wenn man den 6.6'-Dichlor-4.4'-dimethylthio- indigo der Bromierung mit Brom oder Brom abspaltenden Mitteln unterwirft. Die Bro- mierung kann nach den üblichen Verfahren in Nitrobenzol bei höherer Temperatur oder beispielsweise in Chlorsulfonsäure bei niede ren Temperaturen durchgeführt werden.
Der so erhaltene 5.5'-Dibrom-6.6'-dichlor- 4.4'-dimethylthioindigo bildet ein dunkelrotes Pulver, welches sich in Schwefelsäuremono- hydrat und Chlorsulfonsäure mit dunkelgrüner Farbe löst und mit Hydrosulfit und Natron lauge eine goldgelbe güpe bildet, aus der Baumwolle in licht-, koch- und chlorechten rotvioletten Tönen gefärbt wird, die etwas blauer sind als die des nach dem Haupt patent dargestellten Farbstoffes.
<I>Beispiel:</I> 20 Gewichtsteile 6.6'-Dichlor-4.4'-Di- methylthioindigo werden in 300 Gewichts teilen Nitrobenzol suspendiert und mit 18-20 Gewichtsteilen Brom versetzt. Nach kurzem Rühren bei gewöhnlicher Temperatur wird langsam auf 130-140 erhitzt. Bei dieser Temperatur wird solange gehalten, bis die Bromwasserstoffentwicklung zu Ende ist. Man erhitzt dann noch kurze Zeit zum SiedAn und lässt erkalten. Der ausgeschiedene Farb stoff wird filtriert und durch Auskochen mit Sprit vom Nitrobenzol befreit.
Process for the preparation of a vat dye of the thioindigo series. It has been found that a new vat dye of the thioindigo series is obtained if the 6,6'-dichloro-4,4'-dimethylthioindigo is subjected to bromination with bromine or bromine-releasing agents. The brominating can be carried out by the customary processes in nitrobenzene at a higher temperature or, for example, in chlorosulfonic acid at lower temperatures.
The 5.5'-dibromo-6.6'-dichloro-4.4'-dimethylthioindigo obtained in this way forms a dark red powder which dissolves in sulfuric acid monohydrate and chlorosulfonic acid with a dark green color and, with hydrosulfite and sodium hydroxide solution, forms a golden yellow güpe from the cotton in light -, cooking and chlorine-proof red-violet tones that are somewhat bluer than those of the dye represented according to the main patent.
<I> Example: </I> 20 parts by weight of 6.6'-dichloro-4.4'-dimethylthioindigo are suspended in 300 parts by weight of nitrobenzene, and 18-20 parts by weight of bromine are added. After brief stirring at normal temperature, the mixture is slowly heated to 130-140. This temperature is maintained until the evolution of hydrogen bromide has ended. It is then heated to the boil for a short time and allowed to cool. The precipitated dye is filtered and freed from nitrobenzene by boiling with fuel.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE122932X | 1925-06-27 | ||
CH120808T | 1926-06-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH122932A true CH122932A (en) | 1927-10-17 |
Family
ID=25709580
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH122932D CH122932A (en) | 1925-06-27 | 1926-06-25 | Process for the preparation of a vat dye of the thioindigo series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH122932A (en) |
-
1926
- 1926-06-25 CH CH122932D patent/CH122932A/en unknown
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