CH106115A - Process for the production of a new intermediate product. - Google Patents
Process for the production of a new intermediate product.Info
- Publication number
- CH106115A CH106115A CH106115DA CH106115A CH 106115 A CH106115 A CH 106115A CH 106115D A CH106115D A CH 106115DA CH 106115 A CH106115 A CH 106115A
- Authority
- CH
- Switzerland
- Prior art keywords
- mole
- benzidine
- cyanuric chloride
- 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
- C07D251/54—Three nitrogen atoms
- C07D251/70—Other substituted melamines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Coloring (AREA)
Description
Verfahren zur Herstellung eines neuen Zwischenproduktes. Es wurde gefunden, dass man ein neues Zwischenprodukt, das tertiäre Kondensations produkt von einem Mol. Cyanurchlorid mit einem Mol. Benzidin und zwei Mol. 1.8- Aminonaphthol-3.6-disulfosäure, erhält, wenn man auf ein Mol. Cyanurchlorid in beliebiger Reihenfolge ein Mol. Benzidin und zwei Mol. 1 . 8-Aminonaphthol-3.6-disulfosäure einwir ken lässt.
Diese Kondensatiou 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. Benzidin und zwei Mol. 1.8-Aminonaphthol-3.6-di- sulfosäure bildet als Alkalisalz ein in Was ser lösliches, fast farbloses Pulver. Es ent hält kein reaktionsfähiges Chloratom mehr und stellt ein wertvolles Ausgangsmaterial zur Herstellung von Farbstoffen dar.
Beispiel: Zu einer Aufschlemmung von 18,5 Teilen Cyanurchlorid in 1000 Teilen Wasser gibt man eine Lösung von 33,1 Teilen des Di- natriumsalzes der 1.8-Aminonaplhthol-3.6- disulfosäure und rührt, bis die Komponenten verschwunden sind. Hierauf stellt man mit Soda neutral, fügt abermals eine Lösung von 33,1 Teilen des Dinatriumsalzes der 1.8- Aminonaphthol-3.6-disulfosäure hinzu und rührt weiter, bis zum fast vollständigen Ver schwinden des Aminonaphthols. Man neu tralisiert wiederum mit Soda, fügt 18,4 Teile fein pulverisiertes Benzidin hinzu und kocht längere Zeit unter Rühren.
Die klare Lösung wird hierauf ausgesäuert und das tertiäre Kondensationsprodukt von einem Mol. Cya- nurchlorid mit einem Mol. Benzidin und zwei Mol. 2 . 8-Aminonaphthol-3 . 6-disulfosäure filtriert und getrocknet.
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 benzidine and two moles of 1,8-aminonaphthol-3,6-disulfonic acid, is obtained if one mole of cyanuric chloride is used in any order Benzidine and two moles. 8-aminonaphthol-3,6-disulfonic acid can 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 tertiary condensation product of one mole of cyanuric chloride with one mole of benzidine and two moles of 1,8-aminonaphthol-3,6-disulfonic acid forms, as an alkali salt, an almost colorless powder which is soluble in water. It no longer contains a reactive chlorine atom and is a valuable starting material for the production of dyes.
Example: A solution of 33.1 parts of the disodium salt of 1,8-aminonaphthol-3,6-disulfonic acid is added to a suspension of 18.5 parts of cyanuric chloride in 1000 parts of water and the mixture is stirred until the components have disappeared. Then it is made neutral with soda, a solution of 33.1 parts of the disodium salt of 1,8-aminonaphthol-3,6-disulfonic acid is again added and stirring is continued until the aminonaphthol has almost completely disappeared. You neutralize again with soda, add 18.4 parts of finely powdered benzidine and boil for a long time with stirring.
The clear solution is then acidified and the tertiary condensation product of one mole of cyanuric chloride with one mole of benzidine and two moles of 2. 8-aminonaphthol-3. 6-disulfonic acid filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH106115T | 1922-09-07 | ||
CH103430T | 1922-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106115A true CH106115A (en) | 1924-08-01 |
Family
ID=25706414
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106115D CH106115A (en) | 1922-09-07 | 1922-09-07 | Process for the production of a new intermediate product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106115A (en) |
-
1922
- 1922-09-07 CH CH106115D patent/CH106115A/en unknown
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