CH137932A - 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
- CH137932A CH137932A CH137932DA CH137932A CH 137932 A CH137932 A CH 137932A CH 137932D A CH137932D A CH 137932DA CH 137932 A CH137932 A CH 137932A
- Authority
- CH
- Switzerland
- Prior art keywords
- mol
- 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, dass man ein neues Zwischenprodukt erhält, wenn man 1 Mol Cyanurchlorid, 1 Mol 1,8-Aminonaphthol-4,6- disulfosäure und 1 Mol Dehydrothiotoluidin- sulfosäure aufeinander einwirken lässt.
Das sekundäre Kondensationsprodukt aus 1 Mol Cyanurchlorid, 1 Mol 1,8-Aminonaph- thol-4,6-disulfosäure und 1 Mol Dehydrothioto- luidinsulfosäure bildet ein gelbes Pulver, das sich in Sodalösung fast farblos löst. Es be sitzt ausgesprochene Affinität zur Baumwoll- faser und kann auf dieser, zum Beispiel durch Behandeln mit Diazoverbindungen, in Farbstoffe übergeführt werden.
<I>Beispiel</I> Eine feine Suspension von 18,5 Gewichts teilen Cyanurchlorid in Eiswasser wird mit einer neutralen Lösung von 31,9 Gewichts teilen 1,8-Aminonaphthol-4,6-disulfosäitre ver einigt und damit während 1-11z Stunden bei 0 gerührt. Während dieser Zeit lässt man langsam eine Lösung von 5,3 Gewichtsteilen Soda zufliessen. Hierauf fügt man eine neu trale Lösung von 32 Gewichsteilen Dehydro- thiotoluidinsulfosäure zu, steigert die Tempe ratur auf 40 und lässt während 11z Stunden wieder eine Lösung von 5,3 Gewichtsteilen Soda zufliessen.
Aus der schwach gelb ge färbten Lösung kann nach weiterem ein stündigem Rühren das sekundäre Konden sationsprodukt aus 1 Mol Cyanurchlorid, 1 Mol 1,8-Aminonaphthol-4,6-disulfosäure und 1 Mol Dehydrothiotoluidinsulfosäure durch Zufügen von Kochsalz abgeschieden 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-4,6-disulfonic acid and 1 mole of dehydrothiotoluidine sulfonic acid are allowed to act on one another.
The secondary condensation product of 1 mole of cyanuric chloride, 1 mole of 1,8-aminonaphthol-4,6-disulfonic acid and 1 mole of dehydrothiotoluidinsulfonic acid forms a yellow powder which dissolves almost colorlessly in soda solution. It has a pronounced affinity for cotton fibers and can be converted into dyes on this, for example by treatment 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-4,6-disulfonic acid, and thus for 1-11z Stirred at 0 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 increased to 40 and a solution of 5.3 parts by weight of soda is allowed to flow in again over a period of 11z hours.
After a further hour of stirring, the secondary condensation product of 1 mole of cyanuric chloride, 1 mole of 1,8-aminonaphthol-4,6-disulfonic acid and 1 mole of dehydrothiotoluidinsulfonic acid can be deposited by adding sodium chloride from the pale yellow colored solution.
The same product is obtained if the dehydrothiotoluidinsulfonic acid and then the aminonaphthol are allowed to act on the cyanuric chloride.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103430T | 1922-09-07 | ||
CH137932T | 1927-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH137932A true CH137932A (en) | 1930-01-31 |
Family
ID=25706444
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH137932D CH137932A (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) | CH137932A (en) |
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1927
- 1927-10-22 CH CH137932D patent/CH137932A/en unknown
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