CH131494A - Process for the production of a new intermediate product in the tar color industry. - Google Patents
Process for the production of a new intermediate product in the tar color industry.Info
- Publication number
- CH131494A CH131494A CH131494DA CH131494A CH 131494 A CH131494 A CH 131494A CH 131494D A CH131494D A CH 131494DA CH 131494 A CH131494 A CH 131494A
- Authority
- CH
- Switzerland
- Prior art keywords
- mole
- production
- new intermediate
- intermediate product
- acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D251/00—Heterocyclic compounds containing 1,3,5-triazine rings
- C07D251/02—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
- C07D251/12—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D251/26—Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hetero atoms directly attached to ring carbon atoms
- C07D251/40—Nitrogen atoms
- C07D251/48—Two nitrogen atoms
- C07D251/50—Two nitrogen atoms with a halogen atom attached to the third ring carbon atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Zwischenproduktes der Teerfarbenindustrie. Es wurde gefunden, da.ss man ein neues Zwischenprodukt erhält, wenn man 1 Mol. Cyanurchlorid, 1 Mol. 1,8-Aminonaphthol- 3,6--disulfosäure und 1 Mol. Dehydrothioto- luidinsulfosäure aufeinander einwirken lässt.
Das sekundäre Kondensationsprodukt aus 1 Hol. Cyanurchlorid, 1 Mol. 1,8-Amino- naphthol-3,6-disulfosäureund 1 Mol. Dehy- drothiotoluidinsulfosä.ure bildet ein gelbe Pulver, .das sich in Sodalösung fast farblos löst. Es besitzt ausgesprochene Affinität zur Baumwoll,f aser und kann auf dieses Material durch Behandeln mit Diazoverbindungen zu Azofarbstoffen entwickelt werden.
<I>Beispiel:</I> Eine feine Suspension von 18,5 Gewichts teilen Cyanurchlorid in Eiswasser wird mit einer neutralen Lösung von 31,9 Gewichts- teilern 1,8 - Aminonaphthol - 3,6 - disulfosäure vereinigt und damit während 1 bis 11/2 Stunden bei 0 gerührt. Während dieser Zeit lässt man langsam eine Lösung von 5,3 Gewichtsteilen Soda zufliessen. Hierauf fügt man eine neutrale Lösung von 32 Gewichts teilen Dehydrothiotoluidinsulfosäure zu, stei gert die Temperatur auf 40 und lässt wäh rend 11/2 ;Stunden wieder eine Lösung von 5,3 Gewichtsteilen Soda zufliessen.
Aus der schwach gelb gefärbten Lösung kann nach weiterem einstündigen Rühren das sekundäre Kondensationsprodukt aus 1 Mol. Cyanur- chlori.d, 1 Mol. 1,8-Aminonaphthol-3,6-di- sulfo.säure und 1 Mol. Dehydrothiotoluidin- sulfosäure durch Zufügen von Kochsalz ab geschieden werden.
Zum gleichen Produkt gelangt man, wenn man auf das Cyanurchlorid zunächst die Dehydrothiotoluidinsulfosäure und .dann das Aminonaphthol einwirken lässt.
Process for the production of a new intermediate product in the tar color industry. It has been found that a new intermediate is obtained if 1 mole of cyanuric chloride, 1 mole of 1,8-aminonaphthol-3,6-disulfonic acid and 1 mole of dehydrothiotoluidinsulfonic acid are allowed to act on one another.
The secondary condensation product from 1 hol. Cyanuric chloride, 1 mol. 1,8-amino-naphthol-3,6-disulphonic acid and 1 mol. Dehydrothiotoluidinsulphonic acid form a yellow powder which dissolves almost colorlessly in soda solution. It has a pronounced affinity for cotton, fiber and can be developed into azo dyes on this material by treating it with diazo compounds.
<I> Example: </I> A fine suspension of 18.5 parts by weight of cyanuric chloride in ice water is combined with a neutral solution of 31.9 parts by weight of 1.8 - aminonaphthol - 3.6 - disulfonic acid and thus for 1 to Stirred at 0 for 11/2 hours. During this time, a solution of 5.3 parts by weight of soda is allowed to flow in slowly. A neutral solution of 32 parts by weight of dehydrothiotoluidinsulfonic acid is then added, the temperature is raised to 40 and a solution of 5.3 parts by weight of soda is allowed to flow in again for 11/2 hours.
After a further hour of stirring, the secondary condensation product of 1 mole of cyanuric chloride, 1 mole of 1,8-aminonaphthol-3,6-disulfonic acid and 1 mole of dehydrothiotoluidine sulfonic acid can pass through the slightly yellow solution Adding table salt to be divorced.
The same product is obtained if the dehydrothiotoluidinsulfonic acid and then the aminonaphthol are first allowed to act on the cyanuric chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103430T | 1922-09-07 | ||
CH131494T | 1927-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH131494A true CH131494A (en) | 1929-02-15 |
Family
ID=25706443
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH131494D CH131494A (en) | 1922-09-07 | 1927-10-22 | Process for the production of a new intermediate product in the tar color industry. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH131494A (en) |
-
1927
- 1927-10-22 CH CH131494D patent/CH131494A/en unknown
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