[go: up one dir, main page]

DE668967C - Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1) - Google Patents

Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1)

Info

Publication number
DE668967C
DE668967C DEI55930D DEI0055930D DE668967C DE 668967 C DE668967 C DE 668967C DE I55930 D DEI55930 D DE I55930D DE I0055930 D DEI0055930 D DE I0055930D DE 668967 C DE668967 C DE 668967C
Authority
DE
Germany
Prior art keywords
chloro
sulfone
chlorine
oxycyclotetramethylene
preparation
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
DEI55930D
Other languages
German (de)
Inventor
Dr Detlef Delfs
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI55930D priority Critical patent/DE668967C/en
Application granted granted Critical
Publication of DE668967C publication Critical patent/DE668967C/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
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/46Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings substituted on the ring sulfur atom
    • C07D333/48Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings substituted on the ring sulfur atom by oxygen atoms

Landscapes

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

Description

Verfahren zur Darstellung von 3-Chlor-4-oxycyclotetramethylensulfon-(1) Es wurde gefunden, daß durch Einwirkung von unterchloriger Säure bzw. Chlor in Gegenwart von Wasser auf 3 # 4-Diehydrocyclotetram@ethylensulfon-(i) in glatter Ausbeute das 3-Chlor-4-,oxycyclotetramiethylensulfon- (i ) erhalten wird. Die Reaktion kann z. B. in der Form durchgeführt werden, daß man auf die wässerige Lösung bzw. Suspension des Ausgangsprodukts Chlorwasser oder gasförmiges Chlor einwirken läßt. Die Anwesenheit organischer Lösungsmittel, wie z. B. Eisessig oder Alkohol, ist nicht ausgeschlossen. Zwecks Bindung der frei werdenden. Salzsäure können evtl. säurebindende Mittel, wie z. B. Calciumcarbonat, zugesetzt werden. Es empfiehlt sich, die Reaktionstemperatur nicht zu hoch ansteigen zu lassen, da das Ausgangsprodukt zum Zerfall in Butadien und Schwefeldioxyd neigt. Dieser Zerfall ist schon bei i2o° recht lebhaft.Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1) It has been found that by the action of hypochlorous acid or chlorine in the presence of water to 3 # 4-Diehydrocyclotetram @ ethylensulfon- (i) in smooth yield that 3-chloro-4-, oxycyclotetramiethylenesulfone- (i) is obtained. The reaction can e.g. B. be carried out in the form that one on the aqueous solution or suspension of the starting product allows chlorine water or gaseous chlorine to act. The presence organic solvents, such as. B. glacial acetic acid or alcohol is not excluded. For the purpose of binding those who become free. Hydrochloric acid may contain acid-binding agents, such as B. calcium carbonate, can be added. It is recommended that the reaction temperature not to let rise too high, as the starting product breaks down into butadiene and sulfur dioxide tends. This decay is already quite lively at i2o °.

Das Gelingen des neuen Verfahrens war nicht voraussehbar, da das erwähnte Ausgangsprodukt gemäß den Angaben der Literatur bei Verwendung von Brom an Stelle von Chlor in das Dibromid übergeht.The success of the new procedure was not foreseeable, as that mentioned Starting product according to the information in the literature when using bromine instead passes from chlorine to the dibromide.

Das nach dem neuen Verfahren erhaltene 3-Chlor-4-:oxycyclotetramnethyleiisulfon ist in kaltem Wasser ziemlich schwer löslich und fällt daher, zumal wenn keine organischen Lösungsmittel zugegen sind, meist im Laufe der Reaktion aus. Es stellt einen farblosen Körper vom Schmelzpunkt 163 bis 164' dar. Es kann aus Wasser oder Alkohol umkristallisiert werden. Es ist ein wertvolles Zwischenprodukt für die Darstellung von Farbstoffen, Textilhilfsmitteln, Lösungs- und Weichmachungsmitteln.The 3-chloro-4-: oxycyclotetramnethyleiisulfon obtained by the new process is rather sparingly soluble in cold water and therefore falls, especially if no organic Solvents are present, mostly in the course of the reaction. It represents a colorless one Body from melting point 163 to 164 'represents. It can be recrystallized from water or alcohol will. It is a valuable intermediate product for the representation of dyes, Textile auxiliaries, solvents and softeners.

Beispiel i ioo Gewichtsteile 3 # 4-D,ehydrocyclotetramethylensulfon- (i) werden in 5oo Gewichtsteilen Wasser bei 40° gelöst. Dann wird unter Rühren gasförmiges Chlor .eingeleitet. Das Chlor wird sofort gebunden. Durch Kühlung wird die Temperatur auf 4o bis 5o° gehalten. Nach einer Chloraufnahme von 61 Gewichtsteilen ist Chlor in der Lösung nachzuweisen. Das Einleiten wird dann unterbrochen; die Abscheidu,ng des Reaktionsprodukts wird durch Abkühlen auf 15° vervollständigt. Das Reaktionsprodukt wird durch Absaugen von der Mutterlauge getrennt, mit kaltem Wasser gewaschen und getrocknet. Es werden 12o Gewichtsteile 3-Chlor-4-,oxycyclotetram,ethylensulfon erhalten. Weitere Mengen des Umsetzungsproduktes bleiben in der Mutterlauge gelöst.Example i 100 parts by weight of 3 # 4-D, ehydrocyclotetramethylene sulfone (i) are dissolved in 500 parts by weight of water at 40 °. Then it becomes gaseous with stirring Chlorine .introduced. The chlorine is bound immediately. Cooling increases the temperature held at 4o to 5o °. After an uptake of 61 parts by weight of chlorine, it is chlorine to be demonstrated in the solution. The initiation is then interrupted; the separation the reaction product is completed by cooling to 15 °. The reaction product is separated from the mother liquor by suction, washed with cold water and dried. There are 12o parts by weight of 3-chloro-4-, oxycyclotetram, ethylene sulfone obtain. Further amounts of the reaction product remain dissolved in the mother liquor.

Beispiel 2 In 5oo Gewichtsteile auf 85 bis go" erhitztes Wasser läßt man unter lebhaftem Rühren die 5o° warme Lösung von 48o Ge- wichtsteilen 3 # q.-Dehydrocydotetramethylen- sulfon in 6oo Gewichtsteilen Wasser so schnell einlaufen, daß ein gleichzeitig @eing _12 leiteter .starker Chlorstrom gerade verbrau wird. Wenn die Reaktion beendet ist, laje man abkühlen. Es kristallisieren dann 65o Ge', wichtsteile rohes 3-Chlor-q.-'oxycyclotetrame- thylensulfon aus. PATRNTANSYRUCI-I: EXAMPLE 2 In 500 parts by weight of water heated to 85 ° C., the 50 ° warm solution of 48 ° parts by weight 3 # q.-Dehydrocydotetramethylene sulfone in 600 parts by weight of water so run in quickly that a simultaneous @eing _12 Conducted. Strong chlorine stream just consumed will. When the reaction is over, laje to cool down. Then 65o Ge 'crystallize, parts by weight of crude 3-chloro-q .- 'oxycyclotetrame- ethylene sulfone. PATRNTANSYRUCI-I:

Claims (1)

V 1 r, rf,hr,en t _t zur Darstellung von 3-Chlor- teitramethylensulfon-(i), dadurch eck _ et, daß man auf 3 # q.-De-. h.YIK, etrameth),lensulfon-(i) unter- @chl@ 'Säure bzw: Chlor in Gegenwart von asser n einwirken läßt.
V 1 r, rf, hr, en t _t for the representation of 3-chloro teitramethylene sulfone- (i), thereby eck _ et that you can click on 3 # q.-De-. H. YIK , etrameth), lensulfon- (i) under- @ chl @ 'acid or: chlorine in the presence left to act from ater n.
DEI55930D 1936-09-11 1936-09-11 Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1) Expired DE668967C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI55930D DE668967C (en) 1936-09-11 1936-09-11 Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI55930D DE668967C (en) 1936-09-11 1936-09-11 Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1)

Publications (1)

Publication Number Publication Date
DE668967C true DE668967C (en) 1938-12-15

Family

ID=7194245

Family Applications (1)

Application Number Title Priority Date Filing Date
DEI55930D Expired DE668967C (en) 1936-09-11 1936-09-11 Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1)

Country Status (1)

Country Link
DE (1) DE668967C (en)

Similar Documents

Publication Publication Date Title
DE668967C (en) Process for the preparation of 3-chloro-4-oxycyclotetramethylene sulfone- (1)
DE696779C (en) Process for the production of tetrahydrofurans
DE527393C (en) Process for the production of chlorinated phenols
DE601996C (en) Process for the preparation of condensation products from phloroglucine and primary aromatic amines
DE687153C (en) Process for fixing tanning agents in leather
DE441984C (en) Process for developing Kuepen dyes on the fiber
DE562824C (en) Process for the preparation of o-nitrophenyl sulfones and their reduction products
DE894245C (en) Process for the preparation of water-soluble salts of 1,4-diamino-benzenesulfonic acid-N, the amino group of which is substituted in the 1-position of the benzene nucleus by a hydrocarbon radical
DE874309C (en) Process for the production of sulfamic acids and their salts
DE734991C (en) Process for the production of quaternary nitrogen compounds
DE515208C (en) Process for the preparation of m-oxyphenylarylamine carboxylic acids
DE667844C (en) Process for the preparation of amino-substituted arsenobenzene-formaldehyde bisulfite compounds
AT220145B (en) Process for the production of light colored long chain alkylbenzenesulfochlorides
DE719365C (en) Process for the preparation of salts of p-aminophenylstibic acid
DE544621C (en) Process for the preparation of 2- or 3-oxycarbazole
DE900933C (en) Process for the preparation of o-oxyarylcarboxylic acid-ª-naphthylamides
DE480362C (en) Process for the preparation of haloalkylarylcarboxylic acids which contain the halogen in the alkyl group
DE683570C (en) Process for the preparation of water-insoluble derivatives of phenols in the nucleus
DE671841C (en) Process for the preparation of N-alkyl and N-aralkyl compounds of aminoethylphedrine
DE530894C (en) Process for the preparation of aromatic sulfonic acid dihalamides
DE695067C (en) Process for the production of barium trinitroresorcinate with 1 mol of crystal water
DE625585C (en) Process for the production of azo dyes on the fiber
DE566473C (en) Process for the preparation of condensation products of the anthraquinone series
DE448631C (en) Process for the preparation of monoarylbiguanidine salts of substituted dithiocarbamic acids
CH322622A (en) Process for the production of new nicotinic acid benzyl esters