CH106104A - Process for the production of a new intermediate product. - Google Patents

Process for the production of a new intermediate product.

Info

Publication number
CH106104A
CH106104A CH106104DA CH106104A CH 106104 A CH106104 A CH 106104A CH 106104D A CH106104D A CH 106104DA CH 106104 A CH106104 A CH 106104A
Authority
CH
Switzerland
Prior art keywords
sep
acid
production
mol
parts
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 CH106104A publication Critical patent/CH106104A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D251/00Heterocyclic compounds containing 1,3,5-triazine rings
    • C07D251/02Heterocyclic compounds containing 1,3,5-triazine rings not condensed with other rings
    • C07D251/12Heterocyclic 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
    • C07D251/26Heterocyclic 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
    • C07D251/40Nitrogen atoms
    • C07D251/54Three nitrogen atoms
    • C07D251/70Other substituted melamines

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, das tertiäre     K.ondensations-          produkt    von einem     Mol.        Cyanurchlorid    mit  einem     Mol.        1-Aminobenzol-3-1La.rbonsäure    und  zwei     Mol.    1     .8-Aminonaphthol-3.6-disulfo-          säure,    erhält,

   wenn man auf ein     'Mo1.        Cyanur-          ühlorird    in beliebiger Reihenfolge ein     Mol.        1-          A.minobenzol-3-karbonsäure    und zwei Mal.  1.     8-Aminoil.aphthol-3.        6-disiilfosäure    einwir  ken 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.        Cvanurchlorid    mit einem     Mol.        1-Amino-          benzol-3-karbonsäure    und zwei     Mol.        1.8-          Aminonaphtliol-3.6-disulfosäure    bildet als       Alkalis.alz    ein in Wasser lösliches, fast farb  loses Pulver.

   Es enthält kein reaktionsfähiges  Chloratom mehr und stellt ein wertvolles  Ausgangsmaterial zur Herstellung von Farb  stoffen dar.         Beispiel:     31,9 Teile     1.8-A.minonaphthol-3.6-di-          sulfosäure    werden in 500 Teilen Wasser unter  Zusatz von 13,3 Teilen 30     %iger    Natronlauge  gelöst; mit 18,5 Teilen     Cyanurchlorid    versetzt  und gerührt, bis die Komponenten verschwun  den sind.

   Die so erhaltene saure Lösung wird  sehr vorsichtig fast genau neutralisiert und  mit einer Lösung von 31,9 Teilen     1.8-          Aminon.aphthol-3.6-disulfosäure,    13,3 Tei  len 30     %iger    Natronlauge und 30 Teilen     I#a-          triumacetat    in 150 Teilen Wasser versetzt.  Nach einigem Rühren ist die     Aminonaphthol-          sulfosäure    beinahe verschwunden.

   Hierauf  wird mit Soda genau     neutralisiert,    mit einer  Lösung von 14 Teilen     1-Aminobenzol-3-kar-          bonsäure    in 200 Teilen Wasser und     13,3    Tei  len 30     %i,ger    Natronlauge versetzt und län  gere Zeit .am     Rü:ekflusskühler    gekocht.

   Das  tertiäre Kondensationsprodukt von einem       Mol.        Cyanurchlorid,    einem     Mol.        1-Amino-          benzol-3-karbonsäure    und zwei     Mol.        1.8-          Aminonaphth.ol-3.6-disulfosKure    wird hier  auf durch     Aussalzen    und Filtrieren isoliert.



  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 1-aminobenzene-3-1Larboxylic acid and two moles of 1,8-aminonaphthol-3,6-disulfonic acid , receives,

   if you are on a 'Mo1. Cyanuruhlorird in any order one mole. 1- A.minobenzene-3-carboxylic acid and twice. 1. 8-Aminoil.aphthol-3. 6-disilfonic acid can 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 tertiary condensation product of one mole of vanuric chloride with one mole of 1-aminobenzene-3-carboxylic acid and two moles of 1,8-aminonaphthiol-3,6-disulfonic acid forms, as an alkali salt, a water-soluble, almost colorless powder.

   It no longer contains a reactive chlorine atom and is a valuable starting material for the production of dyes. Example: 31.9 parts of 1.8-A.minonaphthol-3.6-disulfonic acid are dissolved in 500 parts of water with the addition of 13.3 parts of 30% strength Sodium hydroxide solution dissolved; mixed with 18.5 parts of cyanuric chloride and stirred until the components have disappeared.

   The acidic solution obtained in this way is very carefully and almost exactly neutralized and treated with a solution of 31.9 parts of 1,8-aminonaphthol-3,6-disulfonic acid, 13.3 parts of 30% strength sodium hydroxide solution and 30 parts of sodium acetate in 150 parts Water added. After some stirring, the aminonaphthol sulfonic acid has almost disappeared.

   It is then precisely neutralized with soda, mixed with a solution of 14 parts of 1-aminobenzene-3-carboxylic acid in 200 parts of water and 13.3 parts of 30% sodium hydroxide solution and boiled on the reflux condenser for a long time.

   The tertiary condensation product of one mole of cyanuric chloride, one mole of 1-aminobenzene-3-carboxylic acid and two moles of 1.8-aminonaphthol-3.6-disulfonic acid is isolated here by salting out and filtering.

 

Claims (1)

EMI0002.0001 <B>PATENTANSPRUCH:</B> <tb> Verfahren <SEP> zur <SEP> Herstellung <SEP> eines <SEP> neuen <tb> Zwischenproduktes, <SEP> des <SEP> tertiären <SEP> Kondensa tionsproduktes <SEP> von <SEP> einem <SEP> Mol. <SEP> CZ <SEP> aniirelilorid <tb> mit <SEP> einem <SEP> Mal. <SEP> 1-Aminoben.zol-3-karbonsätire <tb> und <SEP> zwei <SEP> Mol. <SEP> 1 <SEP> . <SEP> 8-Aminon.a.plithol-3 <SEP> . <tb> sulfosäure, <SEP> dadurch <SEP> geliennzeichziet, <SEP> dass <SEP> man <tb> in <SEP> beliebiger <SEP> Reihenfolge <SEP> auf <SEP> Cyanurchlorid <tb> ein <SEP> Mol. <SEP> 1-Aminobenzol-3-harbonsäure <SEP> und <tb> .wei <SEP> Mol. <SEP> 1 <SEP> . <SEP> 8- <SEP> Aminona.phthol-3 <SEP> . <SEP> 6-cliull'o säure <SEP> einwirken <SEP> lässt. EMI0002.0001 <B> PATENT CLAIM: </B> <tb> Procedure <SEP> for <SEP> production <SEP> of a <SEP> new one <tb> intermediate product, <SEP> of the <SEP> tertiary <SEP> condensation product <SEP> of <SEP> one <SEP> mol. <SEP> CZ <SEP> aniirelilorid <tb> with <SEP> one <SEP> time. <SEP> 1-aminobenzene-3-carbonates <tb> and <SEP> two <SEP> moles. <SEP> 1 <SEP>. <SEP> 8-aminon.a.plithol-3 <SEP>. <tb> sulfonic acid, <SEP> thereby <SEP> geliennzeichziet, <SEP> that <SEP> man <tb> in <SEP> any <SEP> order <SEP> on <SEP> cyanuric chloride <tb> one <SEP> mol. <SEP> 1-aminobenzene-3-harboxylic acid <SEP> and <tb> .wei <SEP> Mol. <SEP> 1 <SEP>. <SEP> 8- <SEP> Aminona.phthol-3 <SEP>. <SEP> 6-cliull'o acid <SEP> allows <SEP> to take effect. EMI0002.0002 Das <SEP> tertiäre <SEP> Kondensationsprodukt <SEP> aus <tb> seinem <SEP> Mol. <SEP> C-,#-anurehlorid <SEP> mit <SEP> einem <SEP> 1,1o1. <SEP> 1 3niinoberizol-3-harbonsäure <SEP> und <SEP> ztvei <SEP> 1,1o1. <tb> 1 <SEP> . <SEP> 8- <SEP> Aminonaphtliol-3 <SEP> . <SEP> 6-disulfosä.ure <SEP> bildet <tb> als <SEP> dlka.lisa.lz <SEP> ein <SEP> in <SEP> Wasser <SEP> lösliches, <SEP> fast <tb> farbloses <SEP> Pulver. <SEP> Es <SEP> enthält <SEP> kein <SEP> reaktions fähiges <SEP> Chloratom <SEP> mehr <SEP> und <SEP> stellt <SEP> ein <SEP> wert volles <SEP> Ausgangsniatera.l <SEP> zur <SEP> Herstellung <SEP> von <tb> Farbstoffen <SEP> dar. EMI0002.0002 The <SEP> tertiary <SEP> condensation product <SEP> <tb> his <SEP> Mol. <SEP> C -, # - anurehlorid <SEP> with <SEP> a <SEP> 1,1o1. <SEP> 1 3niinoberizol-3-harboxylic acid <SEP> and <SEP> ztvei <SEP> 1,1o1. <tb> 1 <SEP>. <SEP> 8- <SEP> aminonaphthiol-3 <SEP>. <SEP> 6-disulfonic acid <SEP> forms <tb> as <SEP> dlka.lisa.lz <SEP> a <SEP> soluble in <SEP> water <SEP>, <SEP> almost <tb> colorless <SEP> powder. <SEP> It <SEP> contains <SEP> no <SEP> reactive <SEP> chlorine atom <SEP> more <SEP> and <SEP> represents <SEP> a <SEP> valuable <SEP> starting niatera.l <SEP > for <SEP> production <SEP> of <tb> dyes <SEP>.
CH106104D 1922-09-07 1922-09-07 Process for the production of a new intermediate product. CH106104A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH106104T 1922-09-07
CH103430T 1922-09-07

Publications (1)

Publication Number Publication Date
CH106104A true CH106104A (en) 1924-08-01

Family

ID=25706403

Family Applications (1)

Application Number Title Priority Date Filing Date
CH106104D CH106104A (en) 1922-09-07 1922-09-07 Process for the production of a new intermediate product.

Country Status (1)

Country Link
CH (1) CH106104A (en)

Similar Documents

Publication Publication Date Title
CH106104A (en) Process for the production of a new intermediate product.
CH106115A (en) Process for the production of a new intermediate product.
CH106076A (en) Process for the production of a new intermediate product.
CH106404A (en) Process for the production of a new intermediate product in the tar color industry.
CH106384A (en) Process for the production of a new intermediate product in the tar color industry.
CH106408A (en) Process for the production of a new intermediate product in the tar color industry.
CH106109A (en) Process for the production of a new intermediate product.
CH106087A (en) Process for the production of a new intermediate product.
CH106376A (en) Process for the production of a new intermediate product in the tar color industry.
CH106075A (en) Process for the production of a new intermediate product.
CH106103A (en) Process for the production of a new intermediate product.
CH106401A (en) Process for the production of a new intermediate product in the tar color industry.
CH106100A (en) Process for the production of a new intermediate product.
CH106385A (en) Process for the production of a new intermediate product in the tar color industry.
CH106074A (en) Process for the production of a new intermediate product.
CH106381A (en) Process for the production of a new intermediate product in the tar color industry.
CH106386A (en) Process for the production of a new intermediate product in the tar color industry.
CH106394A (en) Process for the production of a new intermediate product in the tar color industry.
CH106380A (en) Process for the production of a new intermediate product in the tar color industry.
CH106099A (en) Process for the production of a new intermediate product.
CH106081A (en) Process for the production of a new intermediate product.
CH106117A (en) Process for the production of a new intermediate product.
CH106387A (en) Process for the production of a new intermediate product in the tar color industry.
CH106089A (en) Process for the production of a new intermediate product.
CH106379A (en) Process for the production of a new intermediate product in the tar color industry.