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DE426476C - Process for the preparation of diphenylene sulfide - Google Patents

Process for the preparation of diphenylene sulfide

Info

Publication number
DE426476C
DE426476C DESCH68235D DESC068235D DE426476C DE 426476 C DE426476 C DE 426476C DE SCH68235 D DESCH68235 D DE SCH68235D DE SC068235 D DESC068235 D DE SC068235D DE 426476 C DE426476 C DE 426476C
Authority
DE
Germany
Prior art keywords
preparation
diphenylene sulfide
diphenylene
sulfide
halogen
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
DESCH68235D
Other languages
German (de)
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.)
ALEXANDER SCHOENBERG DR
Original Assignee
ALEXANDER SCHOENBERG DR
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 ALEXANDER SCHOENBERG DR filed Critical ALEXANDER SCHOENBERG DR
Priority to DESCH68235D priority Critical patent/DE426476C/en
Application granted granted Critical
Publication of DE426476C publication Critical patent/DE426476C/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/50Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • C07D333/76Dibenzothiophenes

Landscapes

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

Description

Verfahren zur Darstellung von Diphenylensulfid. In den Berichten 2¢ [18911 Seite 763 ist die Einwirkung eines' halogenhaltigen wasserentziehenden Mittels (Phosphorpentachlorid) auf Diphenylsulfoxvd beschrieben. Diese Einwirkung führte nicht zum Diphenylensulfid. Man erhält jedoch Diphenylensulfid, wenn man mit halogenfreiem wasserentziehenden Mittel arbeitet. .Process for the preparation of diphenylene sulfide. In the reports 2 ¢ [18911 page 763 is the action of a 'halogen-containing dehydrating agent (Phosphorus pentachloride) described on Diphenylsulfoxvd. This impact resulted not to diphenylene sulfide. However, diphenylene sulfide is obtained when using halogen-free dehydrating agent works. .

r. Beispiel.r. Example.

1 Mol. Diphenylsulfoxyd wird in Toluol mit i Mol. Natriumamid 2 Stunden gekocht, die Lösung vom Festen abgetrennt und das Toluol verjagt; es hinterbleibt Diphenylensulfid in einer Ausbeute von 50 Prozent.1 mole of diphenyl sulfoxide is boiled in toluene with 1 mole of sodium amide for 2 hours, the solution is separated from the solid and the toluene is driven off; what remains is diphenylene sulfide in a yield of 50 percent.

z. Beispiel.z. Example.

Main arbeitet wie im Beispiel i, ersetzt jedoch das Natriumamld durch I£aliumamid. 3. Beispiel.Main works as in example i, but replaces the sodium amld with I £ aliumamid. 3rd example.

Man erwärmt ägnimolekulare Mengen Phosphorpentoxyds und Diphenylsulfoxyds, bis Reaktion eintritt, steigert dann die Temperatur nicht mehr, sondern wartet, bis die Reaktion beendigt ist. Man läßt erkalten und zieht die Schmelze mit Benzol aus. Die Benzollösung liefert beim Verjagen des Benzols das Diphenylensulfid. Die Ausbeute ist schlechter als nach Beispiel 1.One heats equal amounts of phosphorus pentoxide and diphenylsulphoxide, until reaction occurs, then the temperature no longer increases, but waits, until the reaction is complete. It is allowed to cool and the melt is drawn in with benzene the end. The benzene solution provides the diphenylene sulfide when the benzene is driven off. the Yield is worse than according to Example 1.

Das Diphenylensulfid soll als Zwischenprodukt für die'Herstellung von Farbstoffen sowie für pharmazeutische Zwecke Verwendung finden.The diphenylene sulfide is said to be an intermediate for the manufacture of dyes and for pharmaceutical purposes.

Claims (1)

PATENT-AN sPRUcH: Verfahren zur Darstellung von Diphenylensulfid, dadurch gekennzeichnet, daß man Diphenylensulfoxyd mit wasserentziehenden halogenfreien Mitteln behandelt.PATENT REQUEST: Process for the preparation of diphenylene sulfide, characterized in that diphenylene sulfoxide is mixed with dehydrating halogen-free Means treated.
DESCH68235D 1923-07-17 1923-07-17 Process for the preparation of diphenylene sulfide Expired DE426476C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DESCH68235D DE426476C (en) 1923-07-17 1923-07-17 Process for the preparation of diphenylene sulfide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DESCH68235D DE426476C (en) 1923-07-17 1923-07-17 Process for the preparation of diphenylene sulfide

Publications (1)

Publication Number Publication Date
DE426476C true DE426476C (en) 1926-03-09

Family

ID=7439364

Family Applications (1)

Application Number Title Priority Date Filing Date
DESCH68235D Expired DE426476C (en) 1923-07-17 1923-07-17 Process for the preparation of diphenylene sulfide

Country Status (1)

Country Link
DE (1) DE426476C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2499186A (en) * 1948-06-17 1950-02-28 Gen Electric 2-vinyldibenzothiophene and method of preparing the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2499186A (en) * 1948-06-17 1950-02-28 Gen Electric 2-vinyldibenzothiophene and method of preparing the same

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