CH106077A - Process for the production of a new intermediate product. - Google Patents
Process for the production of a new intermediate product.Info
- Publication number
- CH106077A CH106077A CH106077DA CH106077A CH 106077 A CH106077 A CH 106077A CH 106077D A CH106077D A CH 106077DA CH 106077 A CH106077 A CH 106077A
- Authority
- CH
- Switzerland
- Prior art keywords
- sulfonic acid
- production
- cyanuric chloride
- intermediate product
- new intermediate
- 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. Es wurde gefunden, dass man ein neues Zwischenprodukt, das sekundäre Kondensa tionsprodukt von einem Mol. Cyanurcblorid mit zwei Mol. 2.5-Aminon.aphthol-7-sulfo- säure, erhält, wenn man auf ein Mol. Cyanür- chloiid zwei Mol. 2.5-Aminon:aphthol-7- sulfosäure einwirken lässt.
Diese Kondensation wird durch Zusam menrühren der Komponenten in einem geeig neten Verdünnungsmittel durchgeführt, und es wurde gefunden, dass als solches Wasser in überraschender Weise sehr gut geeignet ist. Das sekundäre Kondensationsprodukt aus einem Mol. Cy.anurchlorid mit zwei Mol. 2 . 5- Aminonaphthol-7-sulfosäure bildet ein in Wasser leicht lösliches, kristallinisches, fast farbloses Pulver. Es enthält noch ein reak tionsfähiges Chloratom und stellt ein wert volles Ausgangsmaterial zur Herstellung von Farbstoffen dar.
Beispiel: Eine fein verteilte Aufschlemmung von 18,5 Teilen Cyanurchlorid in 1000 Teilen Wasser wird mit Salzsäure schwach sauer ge stellt und nach und nach bei 0 unter Rüh- ren mit einer Lösung von<B>26,2</B> Teilen 2. 5- aminonaphthol-7-sulfosaurem Natrium in 500 Teilen Wasser versetzt, wobei man durch Zugabe von Sololösung (im ganzen 5,3 Teile) die Reaktion immer schwach sauer hält.
Die so erhaltene klare Lösung wird in der Kälte mit Soda neutralisiert und wiederum mit einer weiteren Lösung von<B>26,2</B> Teilen des Natron- salzes der 2.5-Aminonaphthol-7-sulfosäure versetzt. Man rührt, bis die Aminonaphthol- sulfosäure beinahe verschwunden ist, und iso liert das sekundäre Kondensationsprodukt aus einem Mol. Cyanurchlorid und zwei Mol. 2 . 5- Aminonaphthol-7-sulfosäure durch Ansäuern, Aussalzen und Filtrieren.
Process for the production of a new intermediate product. It has been found that a new intermediate product, the secondary condensation product of one mole of cyanuric chloride with two moles of 2.5-aminonaphthol-7-sulfonic acid, is obtained if two moles of 2.5 -Aminon: aphthol-7- sulfonic acid can act.
This condensation is carried out by stirring the components together in a suitable diluent, and it has been found that, surprisingly, water is very suitable as such. The secondary condensation product of one mole of cy.anuric chloride with two moles of 2. 5- Aminonaphthol-7-sulfonic acid forms a crystalline, almost colorless powder that is easily soluble in water. It still contains a reactive chlorine atom and is a valuable starting material for the production of dyes.
Example: A finely divided slurry of 18.5 parts of cyanuric chloride in 1000 parts of water is made slightly acidic with hydrochloric acid and gradually at 0 with stirring with a solution of 26.2 parts 2. 5- aminonaphthol-7-sulphonic acid sodium in 500 parts of water is added, whereby the reaction is always kept slightly acidic by adding solo solution (total of 5.3 parts).
The clear solution obtained in this way is neutralized in the cold with soda, and a further solution of 26.2 parts of the sodium salt of 2,5-aminonaphthol-7-sulfonic acid is added. The mixture is stirred until the aminonaphthol sulfonic acid has almost disappeared, and the secondary condensation product is isolated from one mole of cyanuric chloride and two moles of 2. 5- aminonaphthol-7-sulfonic acid by acidification, salting out and filtering.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103430T | 1922-09-07 | ||
CH106077T | 1922-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106077A true CH106077A (en) | 1924-08-01 |
Family
ID=25706376
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106077D CH106077A (en) | 1922-09-07 | 1922-09-07 | Process for the production of a new intermediate product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106077A (en) |
-
1922
- 1922-09-07 CH CH106077D patent/CH106077A/en unknown
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