CH169565A - Process for the production of a new indigoid dye. - Google Patents
Process for the production of a new indigoid dye.Info
- Publication number
- CH169565A CH169565A CH169565DA CH169565A CH 169565 A CH169565 A CH 169565A CH 169565D A CH169565D A CH 169565DA CH 169565 A CH169565 A CH 169565A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- indigoid dye
- new
- dye
- dimethyl
- Prior art date
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- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen indigoiden Farbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines neuen in- digoiden Farbstoffes, dadurch gekennzeichnet, dass man 4.6-Dimethyl-5-methoxy-3-oxythio- naphthen mit 5.7-Dichlorisatin kondensiert.
Das Produkt verküpt farblos und färbt Baumwolle lebhaft rot in bemerkenswert guter Echtheit. Beispiel: <I>a)</I> Darstellung <I>des</I> Oxythionaphthens <I>:
</I> 3 . 5- Dimethyl-4-aminobenzol-l-sulfosäure wird nach Absatz a) des Beispiels des Hauptpatentes in die 3.5-Dimethyl-4-methoxy-phenyl-l-thio- glykolsäure übergeführt. 25 Teile dieser Thio- glykolsäure werden bei -12 in 450 Teilen Chlorsulfonsäure eingetragen und ungefähr 4 Stunden bei dieser Temperatur gerührt. Es wird auf Eis ausgetragen, das so erhaltene 4. 6-Dim ethyl - 5 - metho$y- 3 - ogythionaphthen abgesaugt, mit Wasser neutral gewaschen und vorsichtig getrocknet.
<I>b)</I> Herstellung <I>des</I> .Farbstoffes <I>:</I> 25 Teile dieses Oxythionaphthens, 22 Teile 5.7-Di- chlorisatin, 500 Teile Eisessig und 0.12 Teile Salzsäure (spez. Crew. =1.19) werden etwa 5 Stunden auf 115-1200 unter Rühren und Rückflusskühlung erwärmt. Der ausgeschiedene Farbstoff wird abgesaugt und aus konzen trierter Schwefelsäure verpastet.
Process for the production of a new indigoid dye. The present patent relates to a process for the production of a new digoid dye, characterized in that 4,6-dimethyl-5-methoxy-3-oxythionnaphthene is condensed with 5,7-dichloroisatin.
The product bundles colorless and dyes cotton vividly red with remarkably good fastness. Example: <I> a) </I> Representation <I> of </I> oxythionaphthene <I>:
</I> 3. 5-dimethyl-4-aminobenzene-1-sulfonic acid is converted into 3,5-dimethyl-4-methoxyphenyl-1-thioglycolic acid according to paragraph a) of the example of the main patent. 25 parts of this thioglycolic acid are introduced into 450 parts of chlorosulfonic acid at -12 and stirred at this temperature for about 4 hours. It is poured onto ice, the 4. 6-dimethyl - 5 - metho $ y - 3 - ogythionaphthene thus obtained is filtered off with suction, washed neutral with water and carefully dried.
<I> b) </I> Production <I> of </I>. Dye <I>: </I> 25 parts of this oxythionaphthene, 22 parts of 5.7-dichloroisatin, 500 parts of glacial acetic acid and 0.12 part of hydrochloric acid (spec . Crew. = 1.19) are heated to 115-1200 with stirring and reflux for about 5 hours. The precipitated dye is suctioned off and pasted from concentrated sulfuric acid.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE169565X | 1932-01-11 | ||
CH166226T | 1932-12-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH169565A true CH169565A (en) | 1934-05-31 |
Family
ID=25718266
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH169565D CH169565A (en) | 1932-01-11 | 1932-12-14 | Process for the production of a new indigoid dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH169565A (en) |
-
1932
- 1932-12-14 CH CH169565D patent/CH169565A/en unknown
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