CH106101A - Process for the production of a new intermediate product. - Google Patents
Process for the production of a new intermediate product.Info
- Publication number
- CH106101A CH106101A CH106101DA CH106101A CH 106101 A CH106101 A CH 106101A CH 106101D A CH106101D A CH 106101DA CH 106101 A CH106101 A CH 106101A
- Authority
- CH
- Switzerland
- Prior art keywords
- mole
- aniline
- production
- sulfonic acid
- cyanuric chloride
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (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. Anilin und zwei Mol. 2.8-Amino- naphthol-6-sulf osäure, erhält, wenn man auf ein Mol. Cya.nurchlorid in beliebiger Reihen folge ein Mol. Anilin und zwei Mol. 2.
8 Aminonaphthol-6-sulfosäure 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 tertiäre Kondensationsprodukt .aus einem Mol. Cyanurchlorid mit einem Mol. Anilin und zwei Mol. 2.8-Aminonaphthol-6-sulfo- säure bildet als Alkalisalz ein in Wasser lös liches, fast farbloses Pulver.
Es enthält kein reaktionsfähiges Chloratom mehr und stellt ein wertvolles Ausgangsmaterial zur Herstel lung von Farbstoffen dar.
<I>Beispiel:</I> Eine fein verteilte Aufschlemmung von 18,5 Teilen Cyanurchlorid in 1000 Teilen Wasser wird mit Salzsäure rohwach sauer ge- stellt und, nach und nach bei 0 unter Rühren mit einer Lösung von 26,2 Teilen 2 . 8-amino- naphthol-6-sulfosaurem Natrium in 500 Tei len Wasser versetzt, wobei span ,durch Zugabe vonSodalösung (im ganzen 5,3 Teile) die Re aktion immer schwach sauer hält.
Die so. er h.altene klare Lösung wird in der Kälte mit Soda neutralisiert und mit einer weiteren Lö sung von 26,2 Teilen des Natronsalzes der 2.8-Aminonaphthol-6-sulfosäure versetzt, wo bei man durch Zugabe von Sodalösung die Reaktion schwach sauer hält.
Ist alle 2. 8 Amino-naphthol-6-sulfosäure verschwunden, so neutralisiert man vollständig, setzt 9,3 Teile Anilin hinzu und kocht eine Stunde am Rückflusskühler. Nachdem man die entstan dene Salzsäure abermals neutralisiert hat, isoliert man das tertiäre Kondensationspro dukt aus einem Mol. Cyanurchlorid, einem Mol. Anilin und zwei Mal. 2.
8-Aminonaph- thol-6-sulfosäure durch Aussalzen und Fil- trieren.
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 aniline and two moles of 2,8-amino-naphthol-6-sulfonic acid, is obtained when one mole of cyanuric chloride is used in any order, one mole of aniline and two moles. 2.
8 aminonaphthol-6-sulfonic acid.
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 aniline and two moles of 2,8-aminonaphthol-6-sulfonic acid forms, as an alkali metal 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.
<I> Example: </I> A finely divided slurry of 18.5 parts of cyanuric chloride in 1000 parts of water is made acidic with raw wax and, gradually at 0 with stirring, with a solution of 26.2 parts of 2. Sodium 8-aminaphthol-6-sulphonic acid is added to 500 parts of water, with the addition of soda solution (5.3 parts in total) always keeping the reaction slightly acidic.
The so. The clear solution that is kept is neutralized in the cold with soda and a further solution of 26.2 parts of the sodium salt of 2,8-aminonaphthol-6-sulfonic acid is added, the reaction being kept slightly acidic by adding soda solution.
If all 2. 8 amino-naphthol-6-sulfonic acid has disappeared, the mixture is completely neutralized, 9.3 parts of aniline are added and the mixture is refluxed for one hour. After the hydrochloric acid formed has been neutralized again, the tertiary condensation product is isolated from one mole of cyanuric chloride, one mole of aniline and twice. 2.
8-aminonaphthol-6-sulfonic acid by salting out and filtering.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103430T | 1922-09-07 | ||
CH106101T | 1922-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106101A true CH106101A (en) | 1924-08-01 |
Family
ID=25706400
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106101D CH106101A (en) | 1922-09-07 | 1922-09-07 | Process for the production of a new intermediate product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106101A (en) |
-
1922
- 1922-09-07 CH CH106101D patent/CH106101A/en unknown
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