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DE1077670B - Process for the production of 2-oxynaphthalene-3-sulfonic acid or its alkali salts and amides - Google Patents

Process for the production of 2-oxynaphthalene-3-sulfonic acid or its alkali salts and amides

Info

Publication number
DE1077670B
DE1077670B DEF26630A DEF0026630A DE1077670B DE 1077670 B DE1077670 B DE 1077670B DE F26630 A DEF26630 A DE F26630A DE F0026630 A DEF0026630 A DE F0026630A DE 1077670 B DE1077670 B DE 1077670B
Authority
DE
Germany
Prior art keywords
sulfonic acid
oxynaphthalene
amides
parts
alkali salts
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.)
Pending
Application number
DEF26630A
Other languages
German (de)
Inventor
Dr Hans Raab
Dr Klaus Boeckmann
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Priority to DEF26630A priority Critical patent/DE1077670B/en
Publication of DE1077670B publication Critical patent/DE1077670B/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof

Landscapes

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

Description

Verfahren zur Herstellung von 2-Oxynaphthalin-3-sulfonsäure bzw. deren Alkalisalzen und Amiden 2-Oxynaphthalin-3-sulfonsäure bzw. deren Alkalisalze und 2-Oxynaphthalin-3-sulfonsäureanilid wurden erstmals von Holt und Mason auf umständlichem und technisch nicht gangbarem Weg aus 2-Methoxy-3-aminonaphthalin hergestellt (Journal of the Chemical Society, London, 1931, S. 378). Process for the production of 2-oxynaphthalene-3-sulfonic acid or their alkali salts and amides 2-oxynaphthalene-3-sulfonic acid or their alkali salts and 2-oxynaphthalene-3-sulfonic acid anilide were first used by Holt and Mason on awkward and a technically impracticable route from 2-methoxy-3-aminonaphthalene (Journal of the Chemical Society, London, 1931, p. 378).

Neuerdings wurde in der französischen Patentschrift 1127 128 eine Methode beschrieben, nach der sich die bei der Sulfierung von 2-Oxvnaphthalin entstehenden geringen Mengen 2-Oxynaphthalin-3-sulfonsäure durch Kristallisation abtrennen lassen sollen. Recently, in French patent specification 1127 128 a Described method according to which the sulfonation of 2-Oxvnaphthalin Allow small amounts of 2-oxynaphthalene-3-sulfonic acid to be separated off by crystallization should.

Auch dieses Verfahren eignet sich nicht zur technischen Gewinnung der 2-Oxynaphthalin-3-sulfonsaure.This process is also unsuitable for technical production of 2-oxynaphthalene-3-sulfonic acid.

Es wurde nun überraschenderweise gefunden, daß sich 2-Oxynaphthalin-3-sulfonsäure bzw. deren Alkalisalze und Amide in guter Ausbeute erhalten lassen, wenn man 2- Chlornaphthalin-3-sulfonsäure bzw. deren entsprechende Derivate mit Alkalihydroxyd in Gegenwart von Wasser auf eine Temperatur von mindestens 1700 C erhitzt. Die Umsetzung erfolgt zur Erzielung ausreichender Temperaturen im Autoklav. wünschtenfalls werden dem Reaktionsgemisch kupferhaltige Katalysatoren wie Kupferpulver oder Kupfer acetat zugesetzt. Als Alkalihydroxyde werden im allgemeinen Natrium- oder Kaliumhydroxyd verwendet. In den folgenden Beispielen stehen Gewichtsteile zu Volumteile im Verhältnis von Gramm zu Millilitern. It has now surprisingly been found that 2-oxynaphthalene-3-sulfonic acid or their alkali salts and amides can be obtained in good yield if you 2- Chloronaphthalene-3-sulfonic acid or its corresponding derivatives with alkali hydroxide heated in the presence of water to a temperature of at least 1700 C. The implementation takes place in the autoclave to achieve sufficient temperatures. will be if desired the reaction mixture copper-containing catalysts such as copper powder or copper acetate added. The alkali hydroxides are generally sodium or potassium hydroxide used. In the following examples, parts by weight are related to parts by volume from grams to milliliters.

Beispiel 1 156Gewichtsteile des Natriumsalzes der 2-Chlorn aphthalin-3-sulfonsäure (etwa 95 0/oil), 700 Volumteile Wasser. 84 Gewichtsteile festes Natriumhydroxyd, 3 Gewiclltsteile Kupferpulver und 0,5 Gewichtsteile Kupferacetat werden in einem Rührautoklav auf 1900 C erwärmt und 10 Stunden bei dieser Temperatur gehalten. Nach dem Abkühlen wird der Inhalt des Autoklavs unter Zusatz von 200 Volumteilen Wasser heiß gelöst und unter Zusatz von Aktivkohle geklärt. Das Filtrat wird mit 300 Gewichtsteilen 500/oiger Essigsäure angesäuert und nach mehrstündigem Rühren das Natriumsalz der 2-Oxynaphthalin-3-sulfonsäure abgesaugt. Example 1 156 parts by weight of the sodium salt of 2-chlorophthalene-3-sulfonic acid (about 95 0 / oil), 700 parts by volume of water. 84 parts by weight of solid sodium hydroxide, 3 parts by weight of copper powder and 0.5 parts by weight of copper acetate are in one The stirred autoclave was heated to 1900 ° C. and kept at this temperature for 10 hours. To cooling the contents of the autoclave with the addition of 200 parts by volume of water Dissolved hot and clarified with the addition of activated charcoal. The filtrate is 300 parts by weight 500 / oiger acetic acid acidified and after several hours of stirring the sodium salt of Sucked off 2-oxynaphthalene-3-sulfonic acid.

Beispiel 2 62 Gewichtsteile 2 - Chlornaphtbalin-3-sulfonsäureanilid (Fp. 1990 C), 380 Volumteile Wasser, 28,8 Ge- wichtsteile festes Natriumhydroxvd, 1 Gewichtsteil Kupferpulver und 0,3 Gewichtsteile Kupferacetat werden im Autoklav unter Rühren auf 1700 C erhitzt und 8 Stunden bei dieser Temperatur gehalten. Der Autoklavinhalt wird nach dem Erkalten und Zusatz von 400 Volumteilen Wasser bis zur Lösung des Reaktionsproduktes erwärmt, unter Zusatz von 3 Gewichtsteilen Aktivkohle geklärt und das 2-Oxynaphthalin-3-sulfanilid mit 20 Voluinprozent Kochsalz als Na-Salz ausgesalzen. Das Na-Salz wird in Wasser gelöst und mit Essigsäure bei 5° C das 2-Oxynaphthalin-3-sulfanilid ausgefällt. Es schmilzt bei 1140 C; nach dem Umkristallisieren aus Dimethylformamid enthält es 1 azol dieses Lösungsmittels und schmilzt bei 149°C. Example 2 62 parts by weight of 2-chloronaphthalene-3-sulfonic acid anilide (Mp. 1990 C), 380 parts by volume of water, 28.8 Ge parts by weight of solid sodium hydroxide, 1 part by weight of copper powder and 0.3 part by weight of copper acetate are placed in the autoclave heated to 1700 ° C. with stirring and held at this temperature for 8 hours. Of the After cooling and adding 400 parts by volume of water, the contents of the autoclave are reduced to heated to dissolve the reaction product, with the addition of 3 parts by weight of activated carbon clarified and the 2-oxynaphthalene-3-sulfanilide with 20 percent by volume table salt as Na salt salted out. The Na salt is dissolved in water and the 2-oxynaphthalene-3-sulfanilide with acetic acid at 5 ° C failed. It melts at 1140 C; after recrystallization from dimethylformamide it contains 1 azole of this solvent and melts at 149 ° C.

PATENTANSPRVCHE 1. Verfahren zur Herstellung von 2-(:)xynaphthalin-3-sulfonsäure bzw. deren Alkalisalzen und Amiden, dadurch gekennzeichnet, daß man 2-Chlornaphthalin-3-sulfonsäure bzw. deren Alkalisalze oder Amide bei einer Temperatur von mindestens 1700 C mit Alkalihydroxyd in Gegenwart von Wasser im Autoklav umsetzt. PATENT CLAIM 1. Process for the preparation of 2 - (:) xynaphthalene-3-sulfonic acid or their alkali salts and amides, characterized in that 2-chloronaphthalene-3-sulfonic acid or their alkali salts or amides at a temperature of at least 1700 C with Reacts alkali hydroxide in the presence of water in the autoclave.

Claims (1)

2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, daß man die Umsetzung in Gegenwart eines kupferhaltigen Katalysators durchführt. 2. The method according to claim 1, characterized in that the Implementation in the presence of a copper-containing catalyst.
DEF26630A 1958-09-18 1958-09-18 Process for the production of 2-oxynaphthalene-3-sulfonic acid or its alkali salts and amides Pending DE1077670B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEF26630A DE1077670B (en) 1958-09-18 1958-09-18 Process for the production of 2-oxynaphthalene-3-sulfonic acid or its alkali salts and amides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF26630A DE1077670B (en) 1958-09-18 1958-09-18 Process for the production of 2-oxynaphthalene-3-sulfonic acid or its alkali salts and amides

Publications (1)

Publication Number Publication Date
DE1077670B true DE1077670B (en) 1960-03-17

Family

ID=7092093

Family Applications (1)

Application Number Title Priority Date Filing Date
DEF26630A Pending DE1077670B (en) 1958-09-18 1958-09-18 Process for the production of 2-oxynaphthalene-3-sulfonic acid or its alkali salts and amides

Country Status (1)

Country Link
DE (1) DE1077670B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0017699A1 (en) * 1979-01-29 1980-10-29 Hoechst Aktiengesellschaft Derivatives of 2-hydroxy-naphthalene and diazo photographic material containing them as coupling components

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0017699A1 (en) * 1979-01-29 1980-10-29 Hoechst Aktiengesellschaft Derivatives of 2-hydroxy-naphthalene and diazo photographic material containing them as coupling components

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