CH297403A - Process for the preparation of a nitroaryl vinyl sulfone. - Google Patents

Process for the preparation of a nitroaryl vinyl sulfone.

Info

Publication number
CH297403A
CH297403A CH297403DA CH297403A CH 297403 A CH297403 A CH 297403A CH 297403D A CH297403D A CH 297403DA CH 297403 A CH297403 A CH 297403A
Authority
CH
Switzerland
Prior art keywords
vinyl sulfone
nitroaryl
parts
preparation
vinyl
Prior art date
Application number
Other languages
German (de)
Inventor
Farbwerke Hoechst Akt Bruening
Original Assignee
Hoechst 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
Application filed by Hoechst Ag filed Critical Hoechst Ag
Publication of CH297403A publication Critical patent/CH297403A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides
    • C07C317/14Sulfones; Sulfoxides having sulfone or sulfoxide groups bound to carbon atoms of six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C315/00Preparation of sulfones; Preparation of sulfoxides
    • C07C315/04Preparation of sulfones; Preparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups

Landscapes

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

Description

  

  Verfahren     zur    Darstellung eines     Nitroaryl-vinylsuNons.            Mononitroaryl    -     vinylsulfone    sind bisher  noch nicht bekannt. Es wurde nun gefunden,       class    man     Mononitroaryl-vinylsulfone    in     guter     bis sehr guter Ausbeute und hoher Reinheit  auf technisch einfache Weise erhalten kann,  wenn man auf     Arylvinylsulfone    der allge  meinen Formel       CHX-CX-SO2-R,     worin R einen aromatischen Rest, beide X  Wasserstoff oder ein X Halogen und das  andere Wasserstoff bedeuten, nitrierende Mit  tel einwirken lässt.

   Die glatte Bildung im Kern  nitrierter     Arylvinylsulfone    ist überraschend,  da beispielsweise die     Nitrierung    von     Vinyl-          benzol    kein     Vinylnitrobenzol,    sondern in der  Hauptsache weitgehende Abbauprodukte lie  fert (vergleiche A. 53, S. 297).  



  Gegenstand des Patentes ist ein Verfahren  zur Herstellung eines     Nitroaryl-v        inylsulfons,     das dadurch     gekennzeichnet    ist, dass man auf       Phenylvinylsulfon    nitrierende Mittel einwir  ken lässt und das so gebildete     Nitrophenyl-          vinylsulfon    isoliert.  



  Das so erhaltene neue     Nitrophenylvinyl-          sulfon    bildet weisse Kristalle,     schmilzt    im  reinen     Zustand    bei 108-109 , löst sich in kon  zentrierter Schwefelsäure und ist in Wasser  unlöslich.

   Es lässt sich aus     Tetrachlorkohlen-          stoff    oder Methanol     umlösen.    Aus der schwe  felsauren Lösung wird die Verbindung durch  Fällen mit Wasser unverändert 7urückerhal-         ten.    Es lässt sich zu     Aminophenylvinylst-tlfon     reduzieren und bildet ein wichtiges Zwischen  produkt für die Herstellung von Farbstoffen,       Polymerisationsprodukten    und Textilhilfsmit  teln.  



  <I>Beispiel 1:</I>  252 Gewichtsteile     Phenylvinylsulfon    wer  den bei 5-10  in 750     Volumteile        100 /oiger     Schwefelsäure eingerührt und gelöst. Dann       lä.sst    man bei der gleichen Temperatur eine       Nitriersäure    aus 95 Gewichtsteilen 100      /o        iger     Salpetersäure und 220 Gewichtsteilen konzen  trierter     Schwefelsäure    langsam     hinzufliessen.     Nach kurzem     Nachrühren    wird das Reaktions  gemisch auf Eiswasser gegossen, die ausge  schiedene, fast farblose Verbindung abgesaugt  und mit Wässer neutral gewaschen.

   Das in  einer Ausbeute von 304 Gewichtsteilen erhal  tene     Nitrophenylvinylsulfon    der wahrschein  lichen Formel:  
EMI0001.0042     
    schmilzt nach dem     LTmlösen    aus Methanol bei  108-109 .  



  <I>Beispiel 2:</I>  16,8 Gewichtsteile     Phenylvinylsulfon    wer  den bei etwa 20-25  in 75     Volumteile          100 /oiger    Schwefelsäure eingerührt und so      in ihr gelöst. Dann trägt man bei der gleichen  Temperatur     portionsweise    9-9,5 Gewichts  teile pulverisiertes N     atriumnitrat    in die Lö  sung ein und rührt bis zur vollständigen Auf  lösung nach. Das Reaktionsgemisch wird auf  Eiswasser gegossen und wie im Beispiel 1 be  schrieben aufgearbeitet. Man erhält das     Nitro-          phenylvinylsulfon    in einer Ausbeute von 20       Clewiehtsteilen.  



  Process for the preparation of a nitroaryl vinyl sulfone. Mononitroaryl vinyl sulfones are not yet known. It has now been found that mononitroaryl vinyl sulfones can be obtained in a technically simple manner in good to very good yield and high purity if one uses aryl vinyl sulfones of the general formula CHX-CX-SO2-R, where R is an aromatic radical, both X. Hydrogen or one X is halogen and the other is hydrogen, nitrating means can act.

   The smooth formation in the core of nitrated aryl vinyl sulfones is surprising since, for example, the nitration of vinyl benzene does not produce vinyl nitrobenzene, but mainly produces extensive degradation products (see A. 53, p. 297).



  The subject of the patent is a process for the production of a nitroaryl vinyl sulfone, which is characterized in that nitrating agents are allowed to act on phenyl vinyl sulfone and the nitrophenyl vinyl sulfone thus formed is isolated.



  The new nitrophenyl vinyl sulfone thus obtained forms white crystals, melts in the pure state at 108-109, dissolves in concentrated sulfuric acid and is insoluble in water.

   It can be converted from carbon tetrachloride or methanol. The compound is retained unchanged from the sulfuric acid solution by precipitation with water. It can be reduced to aminophenylvinylst-tlfon and forms an important intermediate for the manufacture of dyes, polymerisation products and textile auxiliaries.



  <I> Example 1: </I> 252 parts by weight of phenyl vinyl sulfone are stirred into 750 parts by volume of 100% sulfuric acid at 5-10 and dissolved. Then, at the same temperature, a nitrating acid composed of 95 parts by weight of 100% nitric acid and 220 parts by weight of concentrated sulfuric acid is slowly added. After brief stirring, the reaction mixture is poured onto ice water, the separated, almost colorless compound is filtered off with suction and washed neutral with water.

   The nitrophenyl vinyl sulfone of the probable formula obtained in a yield of 304 parts by weight:
EMI0001.0042
    melts at 108-109 after dissolution from methanol.



  <I> Example 2: </I> 16.8 parts by weight of phenylvinylsulfone are stirred into 75 parts by volume of 100% sulfuric acid at around 20-25 parts by volume and thus dissolved in it. Then, at the same temperature, 9-9.5 parts by weight of powdered sodium nitrate are added in portions to the solution and the mixture is stirred until it is completely dissolved. The reaction mixture is poured onto ice water and worked up as described in Example 1 be. The nitrophenyl vinyl sulfone is obtained in a yield of 20 parts by weight.

 

Claims (1)

PATENTANSPRMH Verfahren zur Herstellung eines Nitroa.ryl- vinylsulfons, dadurch gekennzeichnet, dass man auf Phenylvinylsulfon nitrierende Mittel einwirken lässt und das so gebildete Nitro- phenyivinyisulfon isoliert. Das so erhaltene neue Nitroplienyiviiiyl- sulfon bildet weisse Kristalle, schmilzt im rei nen Zustand bei 108-109 , löst sich in kon zentrierter Schwefelsäure und ist. in Wasser unlöslich. PATENT APPLICATION Process for the production of a nitroa.ryl vinyl sulfone, characterized in that nitrating agents are allowed to act on phenyl vinyl sulfone and the nitro phenyl vinyl sulfone thus formed is isolated. The new Nitroplienyiviiiylsulfon thus obtained forms white crystals, melts in the pure state at 108-109, dissolves in concentrated sulfuric acid and is. insoluble in water. Es lässt sich aus Tetraehlorkohlen- stoff oder Methanol umlösen. It can be redissolved from carbon tetrachloride or methanol.
CH297403D 1942-01-29 1943-10-15 Process for the preparation of a nitroaryl vinyl sulfone. CH297403A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE297403X 1942-01-29

Publications (1)

Publication Number Publication Date
CH297403A true CH297403A (en) 1954-03-31

Family

ID=6090672

Family Applications (1)

Application Number Title Priority Date Filing Date
CH297403D CH297403A (en) 1942-01-29 1943-10-15 Process for the preparation of a nitroaryl vinyl sulfone.

Country Status (1)

Country Link
CH (1) CH297403A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1210804B (en) * 1961-07-22 1966-02-17 Basf Ag Process for the preparation of aryl vinyl sulfonic acid esters substituted by nitro groups in the aryl nucleus

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1210804B (en) * 1961-07-22 1966-02-17 Basf Ag Process for the preparation of aryl vinyl sulfonic acid esters substituted by nitro groups in the aryl nucleus

Similar Documents

Publication Publication Date Title
CH297403A (en) Process for the preparation of a nitroaryl vinyl sulfone.
DE889147C (en) Process for the preparation of substituted aryl vinyl sulfones
CH208954A (en) Process for the preparation of a new anthraquinone dye mixture.
DE875201C (en) Process for the preparation of substituted aryl vinyl sulfones
CH297830A (en) Process for the preparation of a mononitroaryl vinyl sulfone.
DE679279C (en) Process for the preparation of a tetraalkylated dinitrobenzene
DE391233C (en) Process for the production of azo dyes
CH180688A (en) Process for the preparation of 2,4-dinitro-3,6-dichloroaniline.
AT206430B (en) Process for the preparation of disulfamylaniline compounds
DE2413189A1 (en) METHOD FOR MANUFACTURING HYDROCHINONS
CH303878A (en) Process for the production of a vinyl sulfone.
CH303518A (en) Process for the preparation of a mononitroaryl vinyl sulfone.
CH136917A (en) Process for the preparation of a mononitro compound of dinaphthylenedioxide.
CH302795A (en) Process for the production of a vinyl sulfone.
CH110109A (en) Process for the preparation of pure 1-nitro-2-methylanthraquinone.
CH211777A (en) Process for the preparation of 2-methyl-4-chloro-6-nitrophenyl-1-trifluoromethylsulfone.
CH322123A (en) Process for the preparation of 2,6-diamino-3,7-dibromo-anthraquinone
CH122247A (en) Process for the preparation of Dibromo-Bz 1-benzanthronylthioglycolic acid.
CH186744A (en) Process for the production of a new anthraquinone dye.
CH120158A (en) Process for the production of a new dye.
CH293617A (en) Process for the preparation of a leuco-sulfuric acid ester salt of an anthraquinone-azo dye.
CH203043A (en) Process for the production of a new dye of the anthraquinone series.
CH211776A (en) Process for the preparation of 2-methyl-4-nitro-5-chlorophenyl-1-trifluoromethylsulfone.
CH160945A (en) Process for the preparation of N-acetyl-2-ethoxy-3-nitrocarbazole.
CH274703A (en) Process for the production of a new dye of the anthraquinone series.