CH130614A - Process for the preparation of a conversion product of peri-cyannaphthalene sulfonic acid. - Google Patents

Process for the preparation of a conversion product of peri-cyannaphthalene sulfonic acid.

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Publication number
CH130614A
CH130614A CH130614DA CH130614A CH 130614 A CH130614 A CH 130614A CH 130614D A CH130614D A CH 130614DA CH 130614 A CH130614 A CH 130614A
Authority
CH
Switzerland
Prior art keywords
preparation
cyannaphthalene
peri
sulfonic acid
conversion product
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellsc Farbenindustrie
Original Assignee
Ig Farbenindustrie Ag
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
Priority claimed from CH128732T external-priority patent/CH128732A/en
Application filed by Ig Farbenindustrie Ag filed Critical Ig Farbenindustrie Ag
Publication of CH130614A publication Critical patent/CH130614A/en

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Description

  

  Verfahren zur Darstellung eines     Emwandlungsproduktes    der     per!-Cyaainaphthalin          sulfosäure.       Vorliegendes Patent bezieht sich auf die       Darstellung    von     6-Xethoxynaphthostyril,    da  durch gekennzeichnet, dass man     6-Oxynapli-          thostyril    mit     methylierenden    Mitteln behan  delt.  



  Das so erhaltene neue     6-Methoxynaphtho-          styril    ist ein fast farbloses Pulver,     das:,     <B>i</B> aus  Benzol umkristallisiert, bei 223  schmilzt. In konzentrierter Schwefelsäure  ist es mit schwach grünlicher Farbe löslich  und wird durch Erwärmen mit verdünnten       Alkalilaugen    zur     6-Methoxy-l-aminonaph-          thalin-8-earbonsäure    verseift.  



  <I>Beispiel:</I>  1. Teil des     Natriumsalzes    von     6-Oxy-          naphthostyril    (vergleiche Patent Nr. 128898)  wird mit 4 Teilen     p-Toluolsulfosä.uremethyl-          ester,        -1    Teilen Soda und etwa 80 Teilen       Trichlorbenzol    auf etwa 160 bis 170   erhitzt,  bis eine Probe nicht mehr     mit    Dia.zoverbin-    Jungen kuppelt. Das     Trichlorbenzol    wird mit  Wasserdampf abgetrieben und der Rückstand  filtriert, gewaschen und getrocknet.



  Process for the preparation of a conversion product of per-cyaainaphthalene sulfonic acid. The present patent relates to the preparation of 6-xethoxynaphthostyril, characterized in that 6-oxynaplothostyril is treated with methylating agents.



  The new 6-methoxynaphthostyril obtained in this way is an almost colorless powder which:, <B> i </B>, recrystallizes from benzene, melts at 223. It is soluble in concentrated sulfuric acid with a pale greenish color and is saponified to 6-methoxy-1-aminonaphthalene-8-carboxylic acid by heating with dilute alkali lye.



  <I> Example: </I> 1. Part of the sodium salt of 6-oxynaphthostyril (see patent no. 128898) is mixed with 4 parts of p-toluenesulfosate, -1 part of soda and about 80 parts of trichlorobenzene to approx 160 to 170 heated until a sample no longer couples with Dia.zoverbin boys. The trichlorobenzene is driven off with steam and the residue is filtered, washed and dried.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung von 6-Meth- oxynaphlhostyril, dadurch gekennzeichnet, dass man 6-Oxynaphthostyril mit methylie- renden Mitteln behandelt. Das so erhaltene neue 6-Methoxynaphtho- styril ist ein fast farbloses Pulver, das, aus Benzol umkristallisiert, bei 223 schmilzt. In konzentrierter Schwefelsäure ist es mit schwach grünlicher Farbe löslich und wird durch Erwärmen mit verdünnten Alkalilaugen zur 6-Methoxy-l-aminonaph- thalin-8-carbonsäure verseift. PATENT CLAIM: Process for the preparation of 6-methoxynaphthostyril, characterized in that 6-oxynaphthostyril is treated with methylating agents. The new 6-methoxynaphthostyrene obtained in this way is an almost colorless powder which, when recrystallized from benzene, melts at 223. It is soluble in concentrated sulfuric acid with a slightly greenish color and is saponified to 6-methoxy-1-aminonaphthalene-8-carboxylic acid by heating with dilute alkali lye.
CH130614D 1925-12-04 1926-11-30 Process for the preparation of a conversion product of peri-cyannaphthalene sulfonic acid. CH130614A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE130614X 1925-12-04
CH128732T CH128732A (en) 1926-07-27 1926-07-27 Process for the preparation of a conversion product of peri-cyannaphthalene sulfonic acid.

Publications (1)

Publication Number Publication Date
CH130614A true CH130614A (en) 1928-12-15

Family

ID=25711148

Family Applications (1)

Application Number Title Priority Date Filing Date
CH130614D CH130614A (en) 1925-12-04 1926-11-30 Process for the preparation of a conversion product of peri-cyannaphthalene sulfonic acid.

Country Status (1)

Country Link
CH (1) CH130614A (en)

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