CH106112A - Process for the production of a new intermediate product. - Google Patents
Process for the production of a new intermediate product.Info
- Publication number
- CH106112A CH106112A CH106112DA CH106112A CH 106112 A CH106112 A CH 106112A CH 106112D A CH106112D A CH 106112DA CH 106112 A CH106112 A CH 106112A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- hol
- toluidine
- production
- intermediate product
- 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)
- Chemical And Physical Treatments For Wood And The Like (AREA)
Description
Verfahren zur Herstellung eines neuen Zwischenproduktes. Es wurde gefunden, dass man ein neues Zwischenprodukt, das sekundäre Kondensa tionsprodukt von einem Hol. Cyanurchlorid mit einem Hol. 1 .8-Aminonaphthol-3. 6-di- sulfosäure und einem Hol. o-Toluidin, erhält, wenn man .auf ein Hol. Cyanurchlorid in be liebiger Reihenfolge ein Hol. 1.8-Amino- naphtho1-3 . 6-clisulfosäure und ein Hol. o-To- luidin einwirken lässt.
Diese Kondensation wird durch Zusam menrühren der Komponenten in einem geeig neten Verdünnungsmittel durchgeführt, und es wurde gefunden, dass Wasser als solches in überraschender Weise sehr gut geeignet ist. Das sekundäre Kondensationsprodukt aus einem Hol. Cyanurchlorid mit einem Hol. 1 . 8-Aminonaphtho1-3 . 6-.disulf osäure und einem Hol. o-Toluidin bildet .als Natriumsalz ein in Wasser lösliches, fast farbloses Pulver.
Es enthält noch ein reaktionsfähiges Chlor atom und stellt ein wertvolles Ausgangsmate- rial zur Herstellung von Farbstoffen dar.
Beispiel: 18,5 Teile Cyanurchlorid werden in 500 Teilen Wasser suspendiert und mit einer Lö- sung von 83,1 Teilen des Dinatriumsalzes -der 1.8-Aminon,aphthol-3.6-disulfosäure in 200 Teilen Wasser in der Kälte verrührt, bis klare Lösung eingetreten ist.
Man fügt nun 10,7 Teile o-Toluidin und 28 Teile kristalli siertes Natriumacetat hinzu und rührt bei gewöhnlicher Temperatur, bis kein o-Toluidin mehr nachweisbar ist. - Das sekundäre Kon densationsprodukt ,aus einem Hol. Cyanur- chlorid, einem Hol. 1. 8-Aminon!aphthol-3 . 6 disnlfosäure und einem Hol. o-Toluidin wird dann durch Aussäurern und Aussalzen iso liert.
Process for the production of a new intermediate product. It was found that a new intermediate product, the secondary condensation product of a Hol. Cyanuric chloride with a hol. 1,8-aminonaphthol-3. 6-disulfonic acid and a hol. o-toluidine, obtained if one .auf a hol. Cyanuric chloride in any order. 1,8-amino-naphtho1-3. 6-clisulfonic acid and a hol. lets o-toluidine act.
This condensation is carried out by stirring the components together in a suitable diluent, and it has been found that water as such is surprisingly very suitable. The secondary condensation product from a haul. Cyanuric chloride with a hol. 1 . 8-aminonaphtho1-3. 6-.disulfonic acid and a hol. As a sodium salt, o-toluidine forms an almost colorless powder which is soluble in water.
It still contains a reactive chlorine atom and is a valuable starting material for the production of dyes.
Example: 18.5 parts of cyanuric chloride are suspended in 500 parts of water and stirred in the cold with a solution of 83.1 parts of the disodium salt of 1.8-aminone, aphthol-3.6-disulfonic acid in 200 parts of water until the solution is clear is.
10.7 parts of o-toluidine and 28 parts of crystallized sodium acetate are then added and the mixture is stirred at ordinary temperature until o-toluidine is no longer detectable. - The secondary condensation product, from a hol. Cyanuric chloride, a hol. 1. 8-aminone! Aphthol-3. 6 disnlfoic acid and one hol. o-Toluidine is then isolated by acidification and salting out.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH106112T | 1922-09-07 | ||
CH103430T | 1922-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106112A true CH106112A (en) | 1924-08-01 |
Family
ID=25706411
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106112D CH106112A (en) | 1922-09-07 | 1922-09-07 | Process for the production of a new intermediate product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106112A (en) |
-
1922
- 1922-09-07 CH CH106112D patent/CH106112A/en unknown
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