CH106092A - Process for the production of a new intermediate product. - Google Patents
Process for the production of a new intermediate product.Info
- Publication number
- CH106092A CH106092A CH106092DA CH106092A CH 106092 A CH106092 A CH 106092A CH 106092D A CH106092D A CH 106092DA CH 106092 A CH106092 A CH 106092A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- phenylenediamine
- production
- mole
- monoformyl
- 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
- C07D251/54—Three nitrogen atoms
- C07D251/70—Other substituted melamines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Developing Agents For Electrophotography (AREA)
Description
Verfahren zur Herstellung eines neuen Zwischenproduktes. Es wurde gefunden, da.ss man ein neues Zwischenprodukt, das tertiäre Kondensations produkt von einem Mol. Cyanurchlorid mit einem Mol. 2.5-Aminoilaphthol-7-sulfosäure und zwei Mol. Monoformyl-1.3-phenylendi- amin, erhält,
wenn man auf ein Mol. Cyanur- chlo@rid in beliebiger Reihenfolge ein Mol. 2.5-Aminonaphth.ol-7-sulfosäure und zwei Mol. Mo@noformyl-1.3-phenylendiamin ein wirken 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 tertiäre Kondensationsprodukt aus einem Mol. Cyanurchlorid mit -einem Mol. 2. 5- Aminonaphthol-7-sulfosäure und zwei Mol. l@Ionoformyl-1.3-phenylendiamin bildet als Alkalisa.lz ein in Wasser lösliches, fast farb loses Pulver.
Es enthält kein reaktions fähiges Chloratom mehr und stellt ein wert volles Ausgangsmaterial zur Herstellung von Farbstoffen dar. <I>Beispiel:</I> Eine fein verteilte Aufschlemmung von 18,5 Teilen Cyanurchlorid in 1000 Teilen Wasser wird nach und nach bei 0 unter Rüh ren mit einer Lösung von 26,2 Teilen .2 . 5- aminonaphthol-7-sulfosaurem Natrium ver setzt, wobei man durch Zugabe von ' Soda lösung (im ganzen 5,3 Teile) die Reaktion stets eben sauer hält.
Die so erhaltene klare Lösung wird nun mit 13,6 Teilen Mono- formyl-1.3-phenylendi,amin versetzt. Man rührt bei Zimmertemperatur, bis das Mo no- fo@rmyl-1.3-phenylendiamin verschwunden ist, indem man weiter die entstehende Salzsäure mit Soda. neutralisiert.
Zu der so erhaltenen Lösung fügt man nun nochmals 13,6 Teile Monoformyl-1.3-phenylendi.amin und kocht zirka eine Stunde am Rückflusskühler. Hier auf wird durch Aussalzen und Fitrieren das tertiäre Kondensationsprodukt aus einem Mol. Cyanurohlorid, einem Mol. 2. 5-amino- naphthol-7-sulfosaurem Natrium und zwei Mol. Monoformyl-1.3-phenylendiamin isoliert.
Process for the production of a new intermediate product. It has been found that a new intermediate product, the tertiary condensation product of one mole of cyanuric chloride with one mole of 2,5-aminoilaphthol-7-sulfonic acid and two moles of monoformyl-1,3-phenylenediamine, is obtained,
if one mole of 2.5-aminonaphth.ol-7-sulfonic acid and two moles of monoformyl-1.3-phenylenediamine are allowed to act on one mole of cyanuric chloride in any order.
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 tertiary condensation product of one mole of cyanuric chloride with one mole of 2. 5- aminonaphthol-7-sulfonic acid and two moles of ionoformyl-1.3-phenylenediamine forms a water-soluble, almost colorless powder as alkali metal.
It no longer contains a reactive chlorine atom and is a valuable starting material for the production of dyes. <I> Example: </I> A finely divided slurry of 18.5 parts of cyanuric chloride in 1000 parts of water is gradually increased to 0 while stirring ren with a solution of 26.2 parts .2. 5- aminonaphthol-7-sulphonic acid sodium ver sets, whereby one keeps the reaction always acidic by adding 'soda solution (total of 5.3 parts).
The clear solution thus obtained is then admixed with 13.6 parts of monoformyl-1,3-phenylenedi, amine. The mixture is stirred at room temperature until the monofo@rmyl-1.3-phenylenediamine has disappeared, by further treating the hydrochloric acid formed with soda. neutralized.
A further 13.6 parts of monoformyl-1,3-phenylenediamine are then added to the solution thus obtained and the mixture is boiled on the reflux condenser for about an hour. Here, the tertiary condensation product is isolated from one mole of cyanuric chloride, one mole of 2.5-aminaphthol-7-sulfonic acid sodium and two moles of monoformyl-1,3-phenylenediamine by salting out and filtering.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103430T | 1922-09-07 | ||
CH106092T | 1922-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106092A true CH106092A (en) | 1924-08-01 |
Family
ID=25706391
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106092D CH106092A (en) | 1922-09-07 | 1922-09-07 | Process for the production of a new intermediate product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106092A (en) |
-
1922
- 1922-09-07 CH CH106092D patent/CH106092A/en unknown
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