CH162351A - Process for the preparation of 1-iodo-8-oxynaphthalene-3,6-disulfonic acid. - Google Patents
Process for the preparation of 1-iodo-8-oxynaphthalene-3,6-disulfonic acid.Info
- Publication number
- CH162351A CH162351A CH162351DA CH162351A CH 162351 A CH162351 A CH 162351A CH 162351D A CH162351D A CH 162351DA CH 162351 A CH162351 A CH 162351A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- oxynaphthalene
- disulfonic acid
- iodo
- acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic 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 Darstellung von 1-Jod-8-ogynaphtalin-3.6-disulfosäure. Das vorliegende Verfahren betrifft die Darstellung von 1-Jod-8-oxynaphtalin-3.6- disulfosäure und ist dadurch gekennzeichnet, dass man 1-Diazo-8.oxynaphtalin-3.6-disulfo- säure mit Jodwasserstoffsäure behandelt.
<I>Beispiel:</I> 40 gr trockene 1-Diazo-8-ogynaphtali ii-3 . 6- disulfosäure werden in 100 em3 Wasser auf geschlemmt und mit 30 cm' konzentrierter Jodwasserstoffsäure versetzt. Während man auf dem Dampfbad die Temperatur langsam steigert, setzt die Stickstoffentwicklung ein; bei<B>70'</B> ist sie beendigt. Die abgekühlte Masse wird ausgeäthert und mit festem Koch salz gesättigt. Den entstandenen Brei presst man nach einiger Zeit ab und kristallisiert aus siedendem Wasser um, wobei beträcht liche Mengen eines hellgrauen in Wasser leicht löslichen Pulvers gewonnen werden.
Das so erhaltene Produkt enthält noch 0,6 % NaCl.
EMI0001.0025
Für <SEP> CioH607JS2Na: <SEP> 28,10% <SEP> J. <SEP> her.
<tb> 27,2% <SEP> J. <SEP> gef. Die neue Verbindung kann als Zwischenpro.. dukt zur Darstellung von Farbstoffen und pharmazeutischen Produkten dienen.
Process for the preparation of 1-iodo-8-ogynaphthalene-3,6-disulfonic acid. The present process relates to the preparation of 1-iodo-8-oxynaphthalene-3.6-disulfonic acid and is characterized in that 1-diazo-8.oxynaphthalene-3.6-disulfonic acid is treated with hydriodic acid.
<I> Example: </I> 40 gr dry 1-diazo-8-ogynaphtali ii-3. 6-disulfonic acid is dissolved in 100 cubic meters of water and treated with 30 cm of concentrated hydriodic acid. While the temperature is slowly increased on the steam bath, the evolution of nitrogen begins; at <B> 70 '</B> it is finished. The cooled mass is etherified and saturated with solid cooking salt. The resulting pulp is pressed after a while and recrystallized from boiling water, with considerable amounts of a light gray powder that is easily soluble in water being obtained.
The product obtained in this way still contains 0.6% NaCl.
EMI0001.0025
For <SEP> CioH607JS2Na: <SEP> 28.10% <SEP> J. <SEP> her.
<tb> 27.2% <SEP> J. <SEP> found. The new compound can be used as an intermediate product for the preparation of dyes and pharmaceutical products.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH162351T | 1932-02-29 | ||
CH159408T | 1933-10-04 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH162351A true CH162351A (en) | 1933-06-15 |
Family
ID=25717226
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH162351D CH162351A (en) | 1932-02-29 | 1932-02-29 | Process for the preparation of 1-iodo-8-oxynaphthalene-3,6-disulfonic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH162351A (en) |
-
1932
- 1932-02-29 CH CH162351D patent/CH162351A/en unknown
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