AT57397B - Process for the preparation of phenylated and substituted, phenylated 6,6'-dichinolyl-4,4'-dicarboxylic acids and homologues. - Google Patents

Process for the preparation of phenylated and substituted, phenylated 6,6'-dichinolyl-4,4'-dicarboxylic acids and homologues.

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Publication number
AT57397B
AT57397B AT57397DA AT57397B AT 57397 B AT57397 B AT 57397B AT 57397D A AT57397D A AT 57397DA AT 57397 B AT57397 B AT 57397B
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AT
Austria
Prior art keywords
phenylated
substituted
dichinolyl
homologues
preparation
Prior art date
Application number
Other languages
German (de)
Original Assignee
Chem Fab Vorm E Schering
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.)
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Application filed by Chem Fab Vorm E Schering filed Critical Chem Fab Vorm E Schering
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Publication of AT57397B publication Critical patent/AT57397B/en

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

   <Desc/Clms Page number 1> 
 



  Verfahren zur Darstellung von   phonyllerten   und substituierten, phenyllerten 6. 6'-Dichinolyl-4.4'-dikarbonsäuren und Homologen. 



   Lässt man Anilin, Benzaldehyd und Brenztraubensäure aufeinander einwirken, so erhält man bekanntlich die 2-Phenylchinolin-4-karbonsäure. In ähnlicher Weise kann man die phenylierton 6. 6'-Dichinolyl-4.4'-dikarbonsäuren und Homologen   darsteHfin, wenn man das   Anilin durch Benzidin oder Tolidin oder Dianisidin ersetzt. Nimmt man an Stelle von Benzaldehyd   substituierte Benzatdobyde, so goiangt, man   zu   entsprochendon Substttutions   produkten. 
 EMI1.1 
 
 EMI1.2 
 
 EMI1.3 
 
 EMI1.4 
 unlöslich und schmilzt bei 248 . 



   Man verfährt analog, wenn man von Tolidin und Dianisidin ausgeht. 



   Beispiel 3 : 106 g   toluidin   und 106 g Benzaldehyd werden in 1200 cm3 absolutem 
 EMI1.5 
 

**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 



  Process for the preparation of phonyl-substituted and substituted, phenyl-substituted 6,6'-dichinolyl-4,4'-dicarboxylic acids and homologues.



   If aniline, benzaldehyde and pyruvic acid are allowed to interact, it is known that 2-phenylquinoline-4-carboxylic acid is obtained. The phenylated 6,6'-dichinolyl-4,4'-dicarboxylic acids and homologues can be prepared in a similar manner if the aniline is replaced by benzidine or tolidine or dianisidine. If, in place of benzaldehyde, substituted benzate dobyds are used, then it is thought that substitution products are used.
 EMI1.1
 
 EMI1.2
 
 EMI1.3
 
 EMI1.4
 insoluble and melts at 248.



   One proceeds analogously if one starts out from tolidine and dianisidine.



   Example 3: 106 g of toluidine and 106 g of benzaldehyde are in 1200 cm3 absolute
 EMI1.5
 

** WARNING ** End of DESC field may overlap beginning of CLMS **.

 

Claims (1)

**WARNUNG** Ende CLMS Feld Kannt Anfang DESC uberlappen**. ** WARNING ** End of CLMS field may overlap beginning of DESC **.
AT57397D 1911-02-28 1912-02-19 Process for the preparation of phenylated and substituted, phenylated 6,6'-dichinolyl-4,4'-dicarboxylic acids and homologues. AT57397B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE57397X 1911-02-28

Publications (1)

Publication Number Publication Date
AT57397B true AT57397B (en) 1913-01-25

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ID=5629147

Family Applications (1)

Application Number Title Priority Date Filing Date
AT57397D AT57397B (en) 1911-02-28 1912-02-19 Process for the preparation of phenylated and substituted, phenylated 6,6'-dichinolyl-4,4'-dicarboxylic acids and homologues.

Country Status (1)

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AT (1) AT57397B (en)

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