CH87882A - Process for the preparation of dibenzylaniline-4 '.4 "-disulfonic acid. - Google Patents

Process for the preparation of dibenzylaniline-4 '.4 "-disulfonic acid.

Info

Publication number
CH87882A
CH87882A CH87882DA CH87882A CH 87882 A CH87882 A CH 87882A CH 87882D A CH87882D A CH 87882DA CH 87882 A CH87882 A CH 87882A
Authority
CH
Switzerland
Prior art keywords
dibenzylaniline
preparation
disulfonic acid
production
uol
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 CH87882A publication Critical patent/CH87882A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/45Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
    • C07C309/46Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton having the sulfo groups bound to carbon atoms of non-condensed six-membered aromatic rings

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur Herstellung von     Dibenzylanilin    4'     #        -i"-disulfosiiure.       Es wurde gefunden, dass     rnan    die     Diben-          zylanilin-4'        #        4"-disulfosäure    in     technisch    sehr  vorteilhafter Weise durch Kondensation von  2     Mol.        benzylchlorid-p-sulfosaurern    Natrium  mit 1     Mol.    Anilin in wässeriger Lösung dar  stellen kann.

       Man    erhält eine Lösung,     welche,     ohne weiteres zur Herstellung von Farbstoffen  verwendet werden kann, oder aus welcher  die     Dibenzylanili -4'        #        4"-disulfosäure        naeh     bekannten Methoden isoliert werden kann.  <I>Beispiel:</I>  9,3 kg Anilin werden in 200 Liter Wasser  suspendiert und bei<B>701</B> unter Rühren nach  einander mit 11 kg Soda und 45 kg     benzyl-          chlorid-p-sulfosaurerrr    Natrium versetzt. Wenn    alles     eingetragen    ist, wird während einer  Viertelstunde gekocht, wobei die     Umsetzung     quantitativ vor sich geht.



  Process for the preparation of dibenzylaniline 4 '# 4 "-disulphonic acid. It has been found that dibenzylaniline-4' # 4" -disulphonic acid can be produced in a technically very advantageous manner by condensation of 2 mol of benzyl chloride-p-sulphonic acid with sodium 1 mol. Aniline in aqueous solution can represent.

       A solution is obtained which can easily be used for the production of dyes, or from which the dibenzylanili -4 '# 4 "-disulfonic acid can be isolated according to known methods. Example: 9.3 kg Aniline is suspended in 200 liters of water and 11 kg of soda and 45 kg of sodium benzyl chloride-p-sulfosaurrrrrrrrrrrrrrrrrrrrrrr soda added at 701. When everything has been added, boiling for a quarter of an hour the implementation is quantitative.

 

Claims (1)

PATENTANSPRUCH: Vurfahren zur Herstellung von Diberrzyl- ,rrrilin-4' # 4"-disulfosäur-e, dadurch gekerrrr- zeichnet, dah 2 Uol. benzylchlorid-p-sulfo- saUres Natrium mit 1 Uol. Anilin in wässe riger Lösung kondensiert wird. Die erhaltene Lösung kann ohne weiteres zur Herstellung von Farbstoffen verwendet werden. PATENT CLAIM: Process for the production of di-benzyl-, rrrilin-4 '# 4 "-disulphonic acid, characterized thereby, that 2 uol. Benzyl chloride-p-sulphonic acid sodium is condensed with 1 uol. Aniline in an aqueous solution. The solution obtained can easily be used for the production of dyes.
CH87882D 1916-01-19 1916-01-19 Process for the preparation of dibenzylaniline-4 '.4 "-disulfonic acid. CH87882A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH85227T 1916-01-19
CH87882T 1916-01-19

Publications (1)

Publication Number Publication Date
CH87882A true CH87882A (en) 1921-01-17

Family

ID=25703444

Family Applications (1)

Application Number Title Priority Date Filing Date
CH87882D CH87882A (en) 1916-01-19 1916-01-19 Process for the preparation of dibenzylaniline-4 '.4 "-disulfonic acid.

Country Status (1)

Country Link
CH (1) CH87882A (en)

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