CH106125A - Process for the preparation of a thioindoxyl derivative. - Google Patents

Process for the preparation of a thioindoxyl derivative.

Info

Publication number
CH106125A
CH106125A CH106125DA CH106125A CH 106125 A CH106125 A CH 106125A CH 106125D A CH106125D A CH 106125DA CH 106125 A CH106125 A CH 106125A
Authority
CH
Switzerland
Prior art keywords
acid
derivative
thioindoxyl
naphthalene
preparation
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 CH106125A publication Critical patent/CH106125A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D335/00Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom
    • C07D335/04Heterocyclic compounds containing six-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D335/08Naphthothiopyrans; Hydrogenated naphthothiopyrans

Description

  

  Verfahren zur Herstellung eines     Thioindogylderivates.       Es wurde     gefunden,    dass man zu einem       Thioindoxylderivat    gelangen kann, wenn  man die     1-Thionaphthol-2-glyoxylsäure,    wel  che man zum     Beispiel    durch Lösen des     1,2-          Thionaphthisatins    des Patentes Nr.

   100851  in     Alkalien    erhalten kann, mit     Monochlor-          essigsWure    zu der     Naphthalin-l-thioglykol-2-          glyoxylsäure    kondensiert, aus dieser Kohlen  oxyd     mittelst    Säuren abspaltet und so in  die     Näphthalin-l-thioglykol-2-karbonsäure     verwandelt und diese dann mit Hilfe von  kondensierend wirkenden     Mitteln    zum     1,2-          Naphththioindoxyl    kondensiert.  



       Beispiel:     214 Teile     1,2-Thionaphthisatin    werden  bei 80   in 10     %iger        Sodalösung    gelöst. Zu  der rotgelben Lösung wird bei gleicher     Tem-          peratr    eine schwach     sodaalkalische    Lösung       von.    140 Teilen     Monochloressigsäure    zu  tropfen gelassen. Es tritt Kondensation un  ter     Entf        ärbung    ein.

   Hierauf lässt man abküh  len und säuert mit verdünnter Salzsäure an;       der    ausfallende Niederschlag wird     abfiltriert.     Die so erhaltene Naphthalin-l-thioglykol-2-         glyoxylsäure    bildet ein farbloses Pulver, das  aus Wasser in schönen Nadeln kristallisiert  und bei 171 bis 172   schmilzt.  



  290 Teile     Naphthalin-l-thioglykol-2-          glyoxylsäure    werden     innert    einer Stunde bei  20 bis 30   in 700 Teile Schwefelsäure von  90 bis 94 % eingetragen. Unter Aufschäumen  geht sie mit dunkelbrauner Farbe in Lösung.  Nach Beendigung der     Kohlenoxydabspaltung     wird das Reaktionsprodukt in Wasser aus  getragen, filtriert,     gewaschen    und getrock  net. Man erhält so die     Naphthalin-l-thio-          glykol-2-karbonsäure    als weisses kristallini  sches Pulver. Nach zweimaligem     Umkristal-          lisieren    aus Wasser schmilzt sie bei 144  bis 145  .  



  262 Teile der so erhaltenen     Naphthalin-          1-thioglylcol-2-karbonsäure    werden in 2000  Teilen     Essigsäureanhydrid    unter Zusatz von  500 Teilen entwässertem     Natriumacetat          einige    Stunden gekocht. Beim Austragen in  Wasser scheidet sich das     acetylierte        1,2-          Naphththioindoxyl    kristallinisch ab. Durch  Erwärmen mit 10     %iger    Natronlauge löst es  sich unter     Verseifung;    durch Säure wird das           l,?-Napliththioindoxyl    ausgefällt.

   Dieses lässt  aus     verdtinnem        Alkohol    oder     Ligroin        umkri-          stallisieren.    Eis bildet feine,     fast    farblose  Nadeln, die bei     1d2      schmelzen.  



  Der     Pingschluss    zum     Naphththioindoxyl,          beziehungsweise    zu dessen     Karbonsäure    kann  auch mit     Alkalien        bewirkt    werden.



  Process for the preparation of a thioindogyl derivative. It has been found that a thioindoxyl derivative can be obtained if 1-thionaphthol-2-glyoxylic acid, which can be obtained, for example, by dissolving the 1,2-thionaphthisatin of patent no.

   100851 can be obtained in alkalis, condensed with monochloroacetic acid to form naphthalene-1-thioglycol-2-glyoxylic acid, split off from this carbon dioxide by means of acids and thus converted into naphthalene-1-thioglycol-2-carboxylic acid and this then with the help of condensing agents to the 1,2-naphththioindoxyl condensed.



       Example: 214 parts of 1,2-thionaphthisatin are dissolved in 10% sodium carbonate solution at 80. At the same temperature, a weakly soda-alkaline solution of. 140 parts of monochloroacetic acid are allowed to drop. Condensation occurs with discoloration.

   It is then allowed to cool down and acidified with dilute hydrochloric acid; the resulting precipitate is filtered off. The naphthalene-1-thioglycol-2-glyoxylic acid thus obtained forms a colorless powder, which crystallizes from water in beautiful needles and melts at 171 to 172.



  290 parts of naphthalene-1-thioglycol-2-glyoxylic acid are introduced within an hour at 20 to 30 in 700 parts of 90 to 94% sulfuric acid. While foaming, it goes into solution with a dark brown color. After the elimination of carbon monoxide has ended, the reaction product is carried out in water, filtered, washed and dried. The naphthalene-1-thioglycol-2-carboxylic acid is thus obtained as a white crystalline powder. After recrystallizing twice from water, it melts at 144 to 145.



  262 parts of the naphthalene-1-thioglylcol-2-carboxylic acid thus obtained are boiled for a few hours in 2000 parts of acetic anhydride with the addition of 500 parts of dehydrated sodium acetate. When discharged into water, the acetylated 1,2-naphthioindoxyl separates out in crystalline form. When heated with 10% sodium hydroxide solution, it dissolves with saponification; the l,? - napliththioindoxyl is precipitated by acid.

   This can be recrystallized from diluted alcohol or ligroin. Ice forms fine, almost colorless needles that melt at 1d2.



  The ping connection to the naphththioindoxyl or its carboxylic acid can also be effected with alkalis.

 

Claims (1)

<B>PATENTANSPRUCH</B> Verfahren zur Darstellung eines Thio- indoxylderivates, dadurch gekennzeichnet, dass man die 1-Thionaplitliol-?-glyoxylsäure mit Monochloressigsäure zu der Naphthalin- 1-thioglykol-2-g1yoxylsäure kondensiert, aus dieser mittelst Säuren Kohlenoxyd abspaltet und so in Naphthalin-l-thiog1ykol-2-h.arbon- säure verwandelt und diese dann mit Hilfe von kondensierend wirkenden Mitteln zum 1,2-LTaphththioindoxyl kondensiert. <B> PATENT CLAIM </B> Process for preparing a thioindoxyl derivative, characterized in that 1-thionaplitliol -? - glyoxylic acid is condensed with monochloroacetic acid to form naphthalene-1-thioglycol-2-g1yoxylic acid, from which carbon oxide is split off by means of acids and so converted into naphthalene-1-thiogolyl-2-hydrogen carboxylic acid and this is then condensed to 1,2-l-phththioindoxyl with the aid of condensing agents.
CH106125D 1922-12-01 1923-02-17 Process for the preparation of a thioindoxyl derivative. CH106125A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH105233T 1922-12-01
CH106125T 1923-02-17

Publications (1)

Publication Number Publication Date
CH106125A true CH106125A (en) 1924-08-01

Family

ID=25706809

Family Applications (1)

Application Number Title Priority Date Filing Date
CH106125D CH106125A (en) 1922-12-01 1923-02-17 Process for the preparation of a thioindoxyl derivative.

Country Status (1)

Country Link
CH (1) CH106125A (en)

Similar Documents

Publication Publication Date Title
CH106125A (en) Process for the preparation of a thioindoxyl derivative.
DE836800C (en) Process for the preparation of 21-oxy-pregnen- (5) -ol- (3) -one- (20) -Abkoemmlingen
CH106127A (en) Process for the preparation of a thioindoxyl derivative.
DE439290C (en) Process for the preparation of naphthooxythiophenes
CH106129A (en) Process for the preparation of a thioindoxyl derivative.
CH106131A (en) Process for the preparation of a thioindoxyl derivative.
CH106411A (en) Process for the preparation of a thioindoxyl derivative.
CH217134A (en) Process for the production of a water-soluble, higher molecular weight, α-substituted benzylamine derivative.
CH106126A (en) Process for the preparation of a thioindoxyl derivative.
AT159956B (en) Process for the preparation of aminobenzenesulfonic acid amide compounds.
CH105233A (en) Process for the preparation of a thioindoxyl derivative.
CH104252A (en) Process for the preparation of di-carbethoxy-di-phenolisatin.
AT34780B (en) Process for the preparation of 3-oxy (1) thionaphthene-2-carboxylic acid (thioindoxylcarboxylic acid) or of mixtures of this acid with 3-oxy (1) thionaphthene (thioindoxyl).
CH106128A (en) Process for the preparation of a thioindoxyl derivative.
DE600923C (en) Process for the production of basic esters of tropic acid
AT205026B (en) Process for the preparation of new α-aroyl-α- (o-carboxybenzoylamino) -acetic acid esters
AT99211B (en) Process for the preparation of o-o-diazyl derivatives of diphenolisatin and its derivatives substituted in the phenol or isatin radical.
DE677327C (en) Process for the preparation of 1, 4-dichloroanthraquinone and its substitution products
DE859154C (en) Process for the preparation of Schiff bases of p-aminosalicylic acid
AT129782B (en) Process for the preparation of 0,0-diacetyldiphenolisatin.
CH106412A (en) Process for the preparation of a thioindoxyl derivative.
CH120705A (en) Process for the preparation of an anthracene derivative.
DE2460421A1 (en) PROCESS FOR THE PRODUCTION OF 2-HYDROXYNAPHTHALIN-3-CARBONIC ACID
CH201833A (en) Process for the production of a new intermediate product.
CH110414A (en) Process for the preparation of an anthracene derivative.