CH176820A - Process for the production of an indigoid vat dye. - Google Patents
Process for the production of an indigoid vat dye.Info
- Publication number
- CH176820A CH176820A CH176820DA CH176820A CH 176820 A CH176820 A CH 176820A CH 176820D A CH176820D A CH 176820DA CH 176820 A CH176820 A CH 176820A
- Authority
- CH
- Switzerland
- Prior art keywords
- production
- vat dye
- dye
- indigoid vat
- indigoid
- Prior art date
Links
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- Coloring (AREA)
Description
Verfahren zur Herstellung eines indigoiden Küpenfarbstoffes. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines indigoiden Küpenfarbstoffes, dadurch gekennzeichnet, dass man 5-Methoxy-6.7-dicbloroxythionaph- then mit 2.1-Naphthoxythiophernanil konden siert.
Der so erhaltene Farbstoff stellt ein braun gefärbtes Pulver dar und färbt Baumwolle aus orangen Küpe in braunen Törnen von guten Echtheiten an. Er löst sich in Schwefel säure mit dunkelblauer Farbe.
<I>Beispiel:</I> 2.3-Dichloranisol-4-sulfosaures Natrium, welches durch Sulfonierung und nachfolgende Alkylierung von 2.3-Dicblorphenol leicht erhältlich ist, wird durch Erhitzen mit Phos- phorpentachlorid in das entsprechende Sulfo- chorid übergeführt. Dieses Sulfochlorid lässt sich ferner auch durch Behandlung von 2.3- Dichloranisol mit Chlorsulfonsäure darstellen.
Das hieraus durch Reduktion erhaltene Mer- kaptan wird in alkalischer Lösung mit Mono chloressigsäure in die Thioglykolsäure über geführt. Die 1-Methoxy-2.3-dichlorbernzol-4- thioglykelsäure zeigt, aus 50 0%iger Essig säure umkristallisiert, einen Schmelzpunkt von 159 0 C. Aus der Thioglykolsäure kann dann mit Hilfe von Phosphortrichlorid und Aluminiumchlorid das 5-lllethöxy-6.7-dichlor- oxythionaphthen dargestellt werden.
12,5 kg 5-13/Iethoxy-6.7-dichloroxythio- naphten und 16;6 kg 2.1-Naphthoxythio- phenanil werden in 1,00 kg Eisessig suspen diert und 6 Stunden unter Rühren auf 100 0 C erhitzt. Nach dem Erkalten wird der gebil dete Farbstoff abgesaugt.
Process for the production of an indigoid vat dye. The present patent relates to a process for the production of an indigoid vat dye, characterized in that 5-methoxy-6.7-dicbloroxythionaph- thene is condensed with 2.1-naphthoxythiophernanil.
The dye thus obtained is a brown-colored powder and dyes cotton from an orange vat in brown grains of good fastness properties. It dissolves in sulfuric acid with a dark blue color.
<I> Example: </I> 2.3-dichloroanisole-4-sulphonic acid sodium, which is easily obtainable by sulphonation and subsequent alkylation of 2,3-dicblophenol, is converted into the corresponding sulphochloride by heating with phosphorus pentachloride. This sulfochloride can also be prepared by treating 2,3-dichloroanisole with chlorosulfonic acid.
The mercaptan obtained from this by reduction is converted into thioglycolic acid in an alkaline solution with monochloroacetic acid. The 1-methoxy-2,3-dichlorobernzene-4-thioglycolic acid shows, recrystallized from 50 0% acetic acid, a melting point of 159 0 C. From the thioglycolic acid the 5-lllethöxy-6.7-dichloro can then with the help of phosphorus trichloride and aluminum chloride oxythionaphthen are represented.
12.5 kg of 5-13 / ethoxy-6.7-dichloroxythio naphthene and 16; 6 kg of 2.1-naphthoxythiophene are suspended in 1.00 kg of glacial acetic acid and heated to 100 ° C. for 6 hours while stirring. After cooling, the dye formed is filtered off with suction.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE176820X | 1933-06-08 | ||
CH174656T | 1934-05-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH176820A true CH176820A (en) | 1935-04-30 |
Family
ID=25719559
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH176820D CH176820A (en) | 1933-06-08 | 1934-05-25 | Process for the production of an indigoid vat dye. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH176820A (en) |
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1934
- 1934-05-25 CH CH176820D patent/CH176820A/en unknown
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