CH177265A - Process for the production of a new intermediate product. - Google Patents

Process for the production of a new intermediate product.

Info

Publication number
CH177265A
CH177265A CH177265DA CH177265A CH 177265 A CH177265 A CH 177265A CH 177265D A CH177265D A CH 177265DA CH 177265 A CH177265 A CH 177265A
Authority
CH
Switzerland
Prior art keywords
amino
nitrobenzoyl
sulfonic acid
oxynaphthalene
manufacture
Prior art date
Application number
Other languages
German (de)
Inventor
Gesellschaft Fuer Chemis Basel
Original Assignee
Chem Ind Basel
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chem Ind Basel filed Critical Chem Ind Basel
Publication of CH177265A publication Critical patent/CH177265A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/041,3-Oxazines; Hydrogenated 1,3-oxazines
    • C07D265/121,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems

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, die     1-(3'Nitrobenzoyl)-ami-          no-4-ainino-5-oxynaphthalin-7-sulfonsäui-e,    er  halten kann, wenn man die OH-Gruppe der       1-Amino-5-oxynaphthalin-7-sulfonsäure    mit  einer     aliphatischen        Carbonsäure,    die höchstens  zwei     Kohlenstoffatome    enthält,     acyliert,    das  so erhaltene Produkt mit einer     Diazoverbin-          dung    vereinigt,

   den so erhaltenen     Azofarb-          stoff    in schwach saurem Medium mit Reduk  tionsmitteln behandelt, den erhältlichen zy  klischen     Iminoäther    der Formel  
EMI0001.0013     
    mit     3-Nitrobenzoylchlorid    kondensiert und    hierauf den zyklischen     Iminoäthei-    durch Be  handeln mit gelinde wirkenden     Verseifungs-          mitteln    spaltet, und die entstandenen     N-Acyl-          verbindung    verseift.  



  Die     1-(3'-Nitrobenzoyl)-amino-4-amino-5-          oxynaphthalin-7-sulfonsäure    bildet ein graues  Pulver, dessen     Alkalisalze    in Wasser leicht  löslich sind. Es ist ein wertvolles Ausgangs  material zur Herstellung von Zwischenpro  dukten oder zur Herstellung von     Farbstoffen.       <I>Beispiel</I>         1-Amino    - 5 -     oxynaphtbalin    -7 -     sulfonsäure     wird auf bekannte Weise in der OH-Gruppe  mit     Essigsäureanhydrid    verestert und alsdann  mit     Diazobenzol    gekuppelt.

   Nach     Aufschlem-          men    des     abfiltrierten    Farbstoffes in verdünn  ter Essigsäure und     successiver    Zugabe von  Zinkstaub bis zur     Entfärbung    scheidet sich  der zyklische     Iminoäther    der     1-Amino-4-ace-          tylamino-5-oxynaphthalin-7-sulfonsäure    der  wahrscheinlichen Formel    
EMI0002.0001     
    als schwach grauer Niederschlag aus, der  durch Filtrieren isoliert wird.  



  Durch Versetzen der neutralen Lösung  der neuen Verbindung mit der äquivalenten  Menge     meta-Nitrobenzoylchlorid    und Na  triumacetat bei etwa<B>300</B> C entsteht die       1-(3'-Nitrobenzoyl)    -     amino    -4-     acetylamino    - 5  ogynaphthalin-7-sulfonsäure, die sich in Form  ihres zyklischen     Iminoäthers    als grauweisse,  schleimige Masse abscheidet.  



  Wird der so erhaltene zyklische     Imino-          äther    der     1-(3'-Nitrobenzoyl)amino-4-acethyl-          amino-5-oxynaphthalin-7-sulfonsäure    kurze  Zeit mit etwa 2     o/oiger    Salzsäure gekocht,  so scheidet sich beim Erkalten die     1-(3'-Nitro-          benzoyl)    -     amino-4-        amino-5-oxynaphthalin-7-          sulfonsäure    als grauer sandiger Niederschlag  aus.



  Process for the production of a new intermediate product. It has been found that a new intermediate, the 1- (3'nitrobenzoyl) -amino-4-ainino-5-oxynaphthalene-7-sulfonic acid, can be obtained if the OH group of the 1- Amino-5-oxynaphthalene-7-sulfonic acid is acylated with an aliphatic carboxylic acid containing at most two carbon atoms, the product thus obtained is combined with a diazo compound,

   the azo dye thus obtained is treated in a weakly acidic medium with reducing agents, the obtainable cyclical imino ether of the formula
EMI0001.0013
    condensed with 3-nitrobenzoyl chloride and then cleaved the cyclic imino ether by treating with mild saponifying agents, and the resulting N-acyl compound saponified.



  1- (3'-Nitrobenzoyl) -amino-4-amino-5-oxynaphthalene-7-sulfonic acid forms a gray powder, the alkali salts of which are easily soluble in water. It is a valuable starting material for the manufacture of intermediate products or for the manufacture of dyes. <I> Example </I> 1-Amino - 5 - oxynaphtbalin -7 - sulfonic acid is esterified in the known manner in the OH group with acetic anhydride and then coupled with diazobenzene.

   After the filtered dye has been suspended in dilute acetic acid and the successive addition of zinc dust until it is discolored, the cyclic imino ether of 1-amino-4-acetylamino-5-oxynaphthalene-7-sulfonic acid of the probable formula separates
EMI0002.0001
    as a pale gray precipitate which is isolated by filtration.



  By adding the equivalent amount of meta-nitrobenzoyl chloride and sodium acetate to the neutral solution of the new compound at about <B> 300 </B> C, 1- (3'-nitrobenzoyl) -amino -4-acetylamino-5-ogynaphthalene-7 is formed -sulphonic acid, which is deposited in the form of its cyclic imino ether as a gray-white, slimy mass.



  If the cyclic imino ether of 1- (3'-nitrobenzoyl) amino-4-acethylamino-5-oxynaphthalene-7-sulphonic acid obtained in this way is boiled with about 2% hydrochloric acid for a short time, the 1st - (3'-Nitrobenzoyl) - amino-4-amino-5-oxynaphthalene-7-sulfonic acid as a gray, sandy precipitate.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines neuen Zwischenproduktes, der 1-(3'-Nitrobenzoyl)- amino-4-amino-5-oxyciaphtbalin-7-sulfonsäure, dadurch gekennzeichnet, dass man die 0R- Gruppe der 1-Amino-5-oxynaphthalin-7-sulfon- säure mit einer aliphatischen Carbonsäure, die höchstens zwei gohlenstoffatome enthält, acyliert, das so erhaltene Produkt mit einer Diazoverbindung vereinigt, den so erhaltenen Azolarbstoff in schwach saurem Medium mit Reduktionsmittel behandelt, PATENT CLAIM: Process for the preparation of a new intermediate, 1- (3'-nitrobenzoyl) - amino-4-amino-5-oxyciaphtbalin-7-sulfonic acid, characterized in that the OR group of 1-amino-5-oxynaphthalene -7-sulfonic acid with an aliphatic carboxylic acid which contains at most two carbon atoms, acylated, the product thus obtained is combined with a diazo compound, the azo material thus obtained is treated in a weakly acidic medium with a reducing agent, den erhältlichen zyklischen Iminoäther der Formel EMI0002.0029 mit 3-Nitrobenzoylchlorid kondensiert und und hierauf den zyklischen Iminoäther durch Behandeln mit gelinde wirkenden Verseifungs- mitteln spaltet, und die entstandene N-Acyl- verbindung verseift. Die 1-(3'-Nitrobenzoyl)-amino-4-amino-5- oxynaphthalin-7-sulfonsäure bildet ein graues Pulver, dessen Alkalisalze in Wasser leicht löslich sind. the available cyclic imino ethers of the formula EMI0002.0029 condensed with 3-nitrobenzoyl chloride and then cleaved the cyclic imino ether by treatment with mild saponifying agents, and saponified the N-acyl compound formed. 1- (3'-Nitrobenzoyl) -amino-4-amino-5-oxynaphthalene-7-sulfonic acid forms a gray powder, the alkali salts of which are easily soluble in water. Es ist ein wertvolles Ausgangs material zur Herstellung von Zwischenpro dukten oder zur Herstellung von Farbstoffen. It is a valuable starting material for the manufacture of intermediate products or for the manufacture of dyes.
CH177265D 1934-07-19 1934-07-19 Process for the production of a new intermediate product. CH177265A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH177265T 1934-07-19

Publications (1)

Publication Number Publication Date
CH177265A true CH177265A (en) 1935-05-31

Family

ID=4427616

Family Applications (1)

Application Number Title Priority Date Filing Date
CH177265D CH177265A (en) 1934-07-19 1934-07-19 Process for the production of a new intermediate product.

Country Status (1)

Country Link
CH (1) CH177265A (en)

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