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DE878718C - Process for the production of copolymers from allylsulfones - Google Patents

Process for the production of copolymers from allylsulfones

Info

Publication number
DE878718C
DE878718C DEC2349D DEC0002349D DE878718C DE 878718 C DE878718 C DE 878718C DE C2349 D DEC2349 D DE C2349D DE C0002349 D DEC0002349 D DE C0002349D DE 878718 C DE878718 C DE 878718C
Authority
DE
Germany
Prior art keywords
parts
allylsulfones
production
copolymers
polymerized
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
DEC2349D
Other languages
German (de)
Inventor
Wilhelm Dr Kunze
Werner Dr Zerweck
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cassella Farbwerke Mainkur AG
Original Assignee
Cassella Farbwerke Mainkur 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 Cassella Farbwerke Mainkur AG filed Critical Cassella Farbwerke Mainkur AG
Priority to DEC2349D priority Critical patent/DE878718C/en
Application granted granted Critical
Publication of DE878718C publication Critical patent/DE878718C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F28/00Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a bond to sulfur or by a heterocyclic ring containing sulfur

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)

Description

Verfahren zur Herstellung von Mischpolymerisaten aus Allylsulfonen Es wurde gefunden, daB man wertvolle hochmolekulare Produkte erhält, wenn man Allylsulfone der allgemeinen Formel CH, =CH-CH2-S02-R, Zwobei R einen Alkyl-, Aralkyl- oder Arylrest bedeutet, in Mischung mit anderen Vinylverbindungen nach an sich bekannten Methoden polymerisiert.Process for the preparation of copolymers from allylsulfones It has been found that valuable high molecular weight products are obtained if allylsulfones of the general formula CH, = CH-CH2-SO2-R, where R is an alkyl, aralkyl or aryl radical, mixed with polymerized other vinyl compounds by methods known per se.

Die hierfür verwendeten Allylsulfone lassen sich leicht, zum Beispiel durch Kondensation von Allylchlorid mit den entsprechenden alkyl-, aralkyl- oder arylsulfinsauren Salzen, darstellen.The allylsulfones used for this can be easily, for example by condensation of allyl chloride with the corresponding alkyl, aralkyl or arylsulfinic salts represent.

Beispiel i 6o Teile Äthylallylsulfon, Kp, n. io5 bis io8°, und q o TeileAcrylsäurenitrilwerden mit etwa ioo Teilen Wasser unter Zusatz von etwas Dibutylnaphthalinsulfonsäure emulgiert, dann fügt man 5 Teile Kaliumpersulfat hinzu und erhitzt etwa 2o Stunden auf etwa 8o°. Das in der Kälte zähe Reaktionsprodukt wird abgetrennt, mit Alkohol verrieben und dekantiert. Es ist in Benzol und Alkoholen unlöslich, dagegen in Aceton und Cyclohexanon löslich und bei Zimmertemperatur noch plastisch. Nach der Analyse hat sich ein Mischpolymerisat aus 43 Teilen Äthylallylsulfon, Kpl mm 88°, und 57 Teilen Acrylsäurenitril gebildet.Example i 6o parts of ethyl allylsulfone, bp, n. Io5 to io8 °, and q o Parts of acrylonitrile are mixed with about 100 parts of water with the addition of a little dibutylnaphthalenesulfonic acid emulsified, then 5 parts of potassium persulfate are added and the mixture is heated for about 20 hours to about 8o °. The reaction product, which is tough in the cold, is separated off with alcohol ground and decanted. It is insoluble in benzene and alcohols, but in acetone and cyclohexanone soluble and still plastic at room temperature. After the analysis has a copolymer of 43 parts of ethyl allyl sulfone, Kpl mm 88 °, and 57 Parts formed acrylonitrile.

Bei einem Ansatz von Zoo Teilen Acrylsäurenitril und 5o Teilen Äthylallylsulfon werden 23 °/o des letzteren einpolymerisiert; das erhaltene farblose Produkt wird bei iq.o bis i5o° plastisch und ist in den genannten Lösungsmitteln unlöslich. Ähnliche Stoffe erhält man bei Verwendung, der entsprechenden Mengen Meth_yl-. allylsulion-; Beispiel 2 ioo Teile Acrylsäurenitrii ,'tind.;@;'`Ieife, :p=Tolvl- allylsulfon, (Ann. 283, [i8947, i83), werden mit etwa, e200- Teilen Wasser unter Zusatz von etwas Dibutyl- "n4plithalinsulfonsäure emulgiert und nach Eintragen von 5 Teilen Kaliumpersulfat etwa 24 Stunden auf 75 bis 8o° erhitzt. Das in fester Form abgeschiedene Produkt wird abgetrennt, mit Alkohol verrührt, ab- gesaugt, gewaschen und getrocknet. Man erhält ein bei 2oo° erweichendes farbloses Mischpolymerisa_ t, das in Benzol unlöslich, dagegen ziemlich schwer in Cyclohexanon löslich ist und durch Mischpolymerisation von 26 Teilen p-Tolylallylsulfon und-.7q.-TeilenLÄeryl- säurenitril entstanden ist. Bei einem Mischungsverhältnis der Polymerisations4 teilnehmer von i : i werden 350j, p-Tolylallylsulfon einpolymerisiert. An Stelle dieses Sulfons kann z. B.@ auch Phenylallylsulfon, (Ann. 283, [i894], i83),_ oder p-Chlorphenylallylsulfon, F.42°, oder BenzyLhltyl- sulfon, F. 64 bis 65°, Journ. Chem. Soc. 685, (i934). unter Bildung ähnlicher Produkte verwendet-werden. Beispiel 3 2o -Teile Acrylsäuremethylester und 2o Teile Äthyl- allylsulfon werden gemischt und mit _o,2 Teilen Benzoylperoxyd_ versetzt,. Die Reaktion wird, durch Erwärmen eingeleitet, nach. ihiern Aufhören wid-hoch etwa 2o Stunden auf etwa ioo° erhitzt. Das farblose Reaktionsprodukt ist in Methanol und Aceton spielend 'löslisli'=üiid 'wind. aüs 'diesen Lösungen mit Wasser gefällt. 'In diesem Mischpolymerisat sind 28 % Äthylallylsulfon einpolymerisiert; es ist ein bei Zimmertemperatur viskoses Produkt. Das mit p-Chlorphenylallylsulfon erhaltene viskose farblose Mischpolymerisat mit 29 °/o dieser Komponente ist in kaltem Methanol schwer, in heißem dagegen leicht löslich.When using zoo parts of acrylonitrile and 50 parts of ethyl allyl sulfone, 23% of the latter is polymerized; the colorless product obtained becomes plastic at iq.o to i50 ° and is insoluble in the solvents mentioned. Similar substances are obtained when using the appropriate amounts of meth_yl-. allylsulion-; Example 2 100 parts of acrylic acid nitride, 'tind.;@;''Ieife,: p = Tolvl- allylsulfone, (Ann. 283, [i8947, i83), with about, e200- parts of water with the addition of some dibutyl "n4plithalinsulfonic acid emulsified and after registration of 5 parts of potassium persulfate for about 24 hours Heated between 75 and 8o °. That which is deposited in solid form Product is separated off, stirred with alcohol, vacuumed, washed and dried. You get a colorless copolymer that softens at 2oo °, which is insoluble in benzene, but quite difficult in Cyclohexanone is soluble and through copolymerization of 26 parts of p-tolylallylsulfone and 7q parts of Läeryl- Acid nitrile is formed. With a mixing ratio of the polymerization 4 participants in i: i will be 350j, p-tolylallylsulfone polymerized. Instead of this sulfone can, for. B. @ also phenylallylsulfone, (Ann. 283, [i894], i83), _ or p-Chlorophenylallylsulfone, melting point 42 °, or BenzyLhlhl- sulfone, m.p. 64 to 65 °, Journ. Chem. Soc. 685, (1934). can be used to form similar products. Example 3 2o parts of methyl acrylate and 2o parts of ethyl allylsulfon are mixed and added with _o.2 parts Benzoylperoxyd_ added ,. The reaction is initiated by heating. Their cessation is heated to about 100 ° for about 20 hours. The colorless reaction product is easy to dissolve in methanol and acetone. like these solutions with water. 'In this copolymer, 28% ethyl allyl sulfone are polymerized; it is a viscous product at room temperature. The viscous colorless copolymer obtained with p-chlorophenylallylsulfone and containing 29% of this component is difficult to dissolve in cold methanol, but readily soluble in hot.

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung von Mischpolymeri-=saten aus -Allylsulfönen, dadurch gekennzeichnet, daß . man Allylsnlfone der allgemeinen Formel CH, = CH-CHz- S02-R, -wobei R einen Alkyl-, Aralkyl- oder Arylrest bedeutet, in Mischung mit anderen Vinylverbindungen nach an sich bekannten Methoden polymerisiert. Angezogene Druckschriften Französische Patentschrift N.r. 855 835.PATENT CLAIM: Process for the production of mixed polymers = saten from -Allylsulfönen, characterized in that. one allyl sulfones of the general formula CH, = CH-CH2-SO2-R, -wherein R denotes an alkyl, aralkyl or aryl radical, polymerized in a mixture with other vinyl compounds according to methods known per se. Referred documents French patent specification No. 855 835.
DEC2349D 1940-08-08 1940-08-08 Process for the production of copolymers from allylsulfones Expired DE878718C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEC2349D DE878718C (en) 1940-08-08 1940-08-08 Process for the production of copolymers from allylsulfones

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEC2349D DE878718C (en) 1940-08-08 1940-08-08 Process for the production of copolymers from allylsulfones

Publications (1)

Publication Number Publication Date
DE878718C true DE878718C (en) 1953-06-05

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DEC2349D Expired DE878718C (en) 1940-08-08 1940-08-08 Process for the production of copolymers from allylsulfones

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2711991A1 (en) * 1977-03-18 1978-09-21 Caloric Ges Apparatebau Product gas with high carbon mon:oxide content - produced by reforming hydrocarbon with carbon di:oxide recovered from burner waste gas

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR855835A (en) * 1938-06-07 1940-05-21 Ig Farbenindustrie Ag Polymerization products, their aqueous emulsions and process for preparing these products

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR855835A (en) * 1938-06-07 1940-05-21 Ig Farbenindustrie Ag Polymerization products, their aqueous emulsions and process for preparing these products

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2711991A1 (en) * 1977-03-18 1978-09-21 Caloric Ges Apparatebau Product gas with high carbon mon:oxide content - produced by reforming hydrocarbon with carbon di:oxide recovered from burner waste gas

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