CH220409A - Process for the preparation of an oxyarylsulfone. - Google Patents
Process for the preparation of an oxyarylsulfone.Info
- Publication number
- CH220409A CH220409A CH220409DA CH220409A CH 220409 A CH220409 A CH 220409A CH 220409D A CH220409D A CH 220409DA CH 220409 A CH220409 A CH 220409A
- Authority
- CH
- Switzerland
- Prior art keywords
- sulfone
- preparation
- oxyarylsulfone
- heated
- melting point
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
Description
Verfahren zur Herstellung eines Ogyarylsulfons. Vorliegendes Patent bezieht sich auf ein Verfahren zur Herstellung eines Oxyarylsul- fons, dadurch gekennzeichnet, dass man ein 2-Halogendiphenylsulfon mit einem alkalisch wirkenden Mittel erhitzt.
Das soerhaltene 2-Oxydiphenylsulfon ist ein farbloser Körper vom Schmelzpunkt 99 bis<B>100'</B> C. Es soll als Zwischenprodukt zur Herstellung von Farbstoffen, Heilmitteln, Textil- und Gerbereihilfsmztteln sowie von synthetischen Harzen Verwendung finden. <I>Beispiel:</I> In eine durch Auflösen von 250 Teilen Kaliumhydroxyd in 1400 Teilen Wasser be reitete Lauge werden 211 Teile 2-Chlordi- phenylsulfon (Fp. 107-1,08 ), erhältlich beispielsweise durch Kondensation von 2-Chlorbenzolsulfochlorid mit Benzol, einge tragen.
Die Mischung wird im Rührautokla- ven etwa 10,Stunden auf 210-220 erhitzt. Man erhält eine hellgefärbte Lösung des Verschmelzunbgsproduktes, die nach Filtra tion am Rührwerk in überschüssige verdünnte Salzsäure eingetragen wird. In fast theoreti scher Ausbeute fällt als weisser Niederschlag das 2-Oxydiphenylsulfon aus, das im Va kuumgetrocknet und aus verdünntem Alko hol umgelöst den Schmelzpunkt 99-100' C zeigt.
Process for the preparation of an ogyaryl sulfone. The present patent relates to a process for the production of an oxyarylsulphone, characterized in that a 2-halodiphenylsulphone is heated with an alkaline agent.
The 2-oxydiphenyl sulfone obtained in this way is a colorless body with a melting point of 99 to <B> 100 '</B> C. It is intended to be used as an intermediate product in the manufacture of dyes, medicinal products, textile and tannery auxiliaries and synthetic resins. <I> Example: </I> In an alkali prepared by dissolving 250 parts of potassium hydroxide in 1400 parts of water, 211 parts of 2-chlorodiphenyl sulfone (melting point 107-1.08), obtainable, for example, by condensation of 2-chlorobenzenesulfochloride, are added with benzene.
The mixture is heated to 210-220 in a stirred autoclave for about 10 hours. A light-colored solution of the fusion product is obtained which, after filtration, is introduced into excess dilute hydrochloric acid on the stirrer. In almost theoretical yield, the 2-oxydiphenylsulfone precipitates out as a white precipitate;
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE220409X | 1939-11-04 | ||
CH218364T | 1940-10-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH220409A true CH220409A (en) | 1942-03-31 |
Family
ID=25726145
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH220409D CH220409A (en) | 1939-11-04 | 1940-10-29 | Process for the preparation of an oxyarylsulfone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH220409A (en) |
-
1940
- 1940-10-29 CH CH220409D patent/CH220409A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH220409A (en) | Process for the preparation of an oxyarylsulfone. | |
CH220407A (en) | Process for the preparation of an oxyarylsulfone. | |
DE648237C (en) | Process for the production of methyl methacrylate | |
CH220406A (en) | Process for the preparation of an oxyarylsulfone. | |
CH220408A (en) | Process for the preparation of an oxyarylsulfone. | |
CH215336A (en) | Process for the preparation of an aminoarylsulfoxide. | |
DE529320C (en) | Process for the preparation of condensation products from amines and aldehydes | |
AT40072B (en) | Process for the preparation of leuco dyes of the indigo group. | |
CH230623A (en) | Process for the production of indole-3-acetic acid. | |
CH220410A (en) | Process for the preparation of an oxyarylsulfone. | |
CH141752A (en) | Process for the production of a halogen derivative of terephthalic acid. | |
CH188770A (en) | Process for the preparation of octadecylaminoacetic acid. | |
CH245679A (en) | Process for the preparation of a 4-chloro-benzenesulfonamide. | |
CH209509A (en) | Process for the preparation of an aminoarylsulfone. | |
CH209508A (en) | Process for the preparation of an aminoarylsulfone. | |
CH235928A (en) | Process for the production of a condensation product. | |
CH296241A (en) | Process for the preparation of N-acrylaminoacetic acid. | |
CH182586A (en) | Process for the preparation of a heterocyclic amino compound. | |
CH201175A (en) | Process for the preparation of a 4-oxy-naphthostyril body. | |
CH182587A (en) | Process for the preparation of a heterocyclic amino compound. | |
CH209510A (en) | Process for the preparation of an aminoarylsulfone. | |
CH231643A (en) | Process for the preparation of a carboxyl-containing degradation product. | |
CH154817A (en) | Process for the preparation of a new conversion product of 1,2-anthraquinone-thioglycol-carboxylic acid. | |
CH184474A (en) | Process for the preparation of a heterocyclic compound. | |
CH201174A (en) | Process for the preparation of a 4-oxy-naphthostyril body. |