CH220403A - Process for the production of a new intermediate product. - Google Patents
Process for the production of a new intermediate product.Info
- Publication number
- CH220403A CH220403A CH220403DA CH220403A CH 220403 A CH220403 A CH 220403A CH 220403D A CH220403D A CH 220403DA CH 220403 A CH220403 A CH 220403A
- Authority
- CH
- Switzerland
- Prior art keywords
- new intermediate
- intermediate product
- amino
- production
- parts
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
- C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C275/40—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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, den N-Phenyl-N'-(2,5-di- äthoxy-4-amino)-phenylharxistoff, erhält, wenn man auf 1 Mol 1-Amino-4-acetylamino-2,5- diäthoxybenzol 1 Mol Phenylisocyanat ein wirken lässt und hierauf das entstandene Pro dukt mit einem Verseifungsmittel behandelt.
Das neue Zwischenprodukt bildet einen kristallinischen Körper, der sich unter Zusatz von Salzsäure in Wasser diazotieren lässt. Diese Diazoverbindung gibt mit Aryliden der 2,3-Oxynaphthoesäure Farbstoffe, welche, auf der Faser erzeugt, diese in echten blauen Tönen färben.
<I>Beispiel:</I> 23,8 Teile 1-Amino-4-acetylamino-2,5-di- äthoxybenzol werden in 400 Teilen siedendem Benzol gelöst und mit einer Lösung von 12 Teilen Phenylisocyanat in 50 Teilen Benzol auf einmal versetzt. Nach einigen Sekunden erstarrt alles zu einem dicken Brei. Nach dem Abkühlen wird das Umsetzungsprodukt ab filtriert. Zur Abspaltung der Acetylgruppe werden 35,7 Teile davon mit 450 Teilen Al kohol und 14 Teilen 33 /oiger Chlorwasser- stoffsäure während 2 Stunden erhitzt. Nach und nach geht alles in Lösung.
Durch Ein dampfen im Vakuum bei 70-80o wird das weisse kristalline Chlorhydrat des N-Phenyl- N'- (2,5- diäthoxy- 4 - amino) - phenylharnstoffe s erhalten.
Process for the production of a new intermediate product. It has been found that a new intermediate, the N-phenyl-N '- (2,5-diethoxy-4-amino) -phenylharxistoff, is obtained when 1-amino-4-acetylamino-2 , 5- diethoxybenzene 1 mole of phenyl isocyanate can act and then treated the resulting product with a saponifying agent.
The new intermediate product forms a crystalline body that can be diazotized in water with the addition of hydrochloric acid. This diazo compound, together with arylides of 2,3-oxynaphthoic acid, gives dyes which, when produced on the fiber, dye them in true blue tones.
<I> Example: </I> 23.8 parts of 1-amino-4-acetylamino-2,5-diethoxybenzene are dissolved in 400 parts of boiling benzene, and a solution of 12 parts of phenyl isocyanate in 50 parts of benzene is added all at once . After a few seconds everything solidifies into a thick paste. After cooling, the reaction product is filtered off. To split off the acetyl group, 35.7 parts of it are heated with 450 parts of alcohol and 14 parts of 33% hydrochloric acid for 2 hours. Little by little everything goes into solution.
The white crystalline hydrochloride of N-phenyl-N'- (2,5-diethoxy-4-amino) -phenylureas is obtained by evaporating in vacuo at 70-80o.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH220403T | 1940-07-20 | ||
CH217227T | 1940-07-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH220403A true CH220403A (en) | 1942-03-31 |
Family
ID=25725916
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH220403D CH220403A (en) | 1940-07-20 | 1940-07-20 | Process for the production of a new intermediate product. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH220403A (en) |
-
1940
- 1940-07-20 CH CH220403D patent/CH220403A/en unknown
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