CH106402A - Process for the production of a new intermediate product in the tar color industry. - Google Patents
Process for the production of a new intermediate product in the tar color industry.Info
- Publication number
- CH106402A CH106402A CH106402DA CH106402A CH 106402 A CH106402 A CH 106402A CH 106402D A CH106402D A CH 106402DA CH 106402 A CH106402 A CH 106402A
- Authority
- CH
- Switzerland
- Prior art keywords
- mole
- amino
- cyanuric chloride
- new intermediate
- production
- 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
- C07D251/42—One nitrogen atom
- C07D251/44—One nitrogen atom with halogen atoms attached to the two other ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines neuen Zwischenproduktes der Teerfarbenindustrie. Es wurde gefunden, d.ass man ein neues Zwischenprodukt, das primäre Kondensations produkt von einem Mol. Cyanurchlorid mit einem Mol. 1-Amino - 3 - nitrobenzol, erhält, wenn man auf ein Mol. Cyanurchlorid ein Hol. 1-Amino-3-nitrobenzol 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 primäre Kondensationsprodukt .aus einem Mol. Cya.nurchlorid mit einem 112o1. 1-Amino- 3-nitrobenzol bildet ein in Wasser unlösliches, fast farbloses Pulver. Aus Aceton umgelöst, schmilzt es bei 202'.
Beim Übergiessen mit 10 %iger Natronlauge wandelt es sich in .einen voluminösen orangegefärbten Körper um, ,der sich in kaltem Wasser mit grünlichgelber Farbe löst. Es enthält noch zwei reaktions fähige Chloratome und bildet ein wertvolles Ausgangsmaterial zur Herstellung von Farb stoffen. <I>Beispiel:</I> Eine feine Suspension von 18,6 Teilen Cyanurchlorid wird unter Rühren mit einer Lösung von 17,4 Teilen 1-Amino-3-nitroben- zöl versetzt und so lange gerührt, bis das 1- Amino-3-nitrobenzol fast verschwunden ist.
Der gebildete kristallinische Niederschlag wird dann filtriert und getrocknet.
Process for the production of a new intermediate product in the tar color industry. It has been found that a new intermediate, the primary condensation product of one mole of cyanuric chloride with one mole of 1-amino-3-nitrobenzene, is obtained when one mole of cyanuric chloride is used. 1-Amino-3-nitrobenzene is allowed to 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 primary condensation product of one mole of cyano chloride with a 112o1. 1-Amino-3-nitrobenzene forms an almost colorless powder which is insoluble in water. Dissolved from acetone, it melts at 202 '.
When 10% sodium hydroxide solution is poured over it, it changes into a voluminous orange-colored body, which dissolves in cold water with a greenish-yellow color. It still contains two reactive chlorine atoms and is a valuable starting material for the production of dyes. <I> Example: </I> A fine suspension of 18.6 parts of cyanuric chloride is mixed with a solution of 17.4 parts of 1-amino-3-nitrobenzöl while stirring and the mixture is stirred until the 1- amino- 3-nitrobenzene has almost disappeared.
The crystalline precipitate formed is then filtered and dried.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH103430T | 1922-09-07 | ||
CH106402T | 1922-09-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH106402A true CH106402A (en) | 1924-08-16 |
Family
ID=25706432
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH106402D CH106402A (en) | 1922-09-07 | 1922-09-07 | Process for the production of a new intermediate product in the tar color industry. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH106402A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3054793A (en) * | 1956-06-15 | 1962-09-18 | Ici Ltd | New water soluble nitro dyestuffs containing a mono- or di-halogeno-1:3:5-triazinyl-(2)-amino group |
-
1922
- 1922-09-07 CH CH106402D patent/CH106402A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3054793A (en) * | 1956-06-15 | 1962-09-18 | Ici Ltd | New water soluble nitro dyestuffs containing a mono- or di-halogeno-1:3:5-triazinyl-(2)-amino group |
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