CH161481A - Process for the preparation of 2,3-dimethylindole-6-sulfonic acid. - Google Patents
Process for the preparation of 2,3-dimethylindole-6-sulfonic acid.Info
- Publication number
- CH161481A CH161481A CH161481DA CH161481A CH 161481 A CH161481 A CH 161481A CH 161481D A CH161481D A CH 161481DA CH 161481 A CH161481 A CH 161481A
- Authority
- CH
- Switzerland
- Prior art keywords
- dimethylindole
- sulfonic acid
- preparation
- condensation
- acid
- Prior art date
Links
Landscapes
- Indole Compounds (AREA)
Description
Verfahren zur Darstellung der 2.3-Dimethylindol-6-sulfonsäure. Es wurde (yefunden, dass man die 2.3 1.)imethylindol-6-sulfosäure erhält, wenn man m-Phenylhydrazinsulfosäure mit Methyl- äthylketon kondensiert. Als Kondensations mittel kann man hierbei die bekannten Kon densationsmittel anwenden: beispielsweise Eisessig. Man kann aber auch in neutraler Lösung arbeiten oder in schwachsaurer, wie verdünnter Essigsäure. Das neue Produkt kristallisiert in Form des Natriumsalzes in kleinen weissen Kriställchen. Es soll als Zwischenprodukt bei der Herstellung von Farbstoffen Verwendung finden.
Beispiel: 19 kg m-Phenylhydrazinsulfosäure wer den in 100 Liter Wasser mit 7,5 kg Methyl- äthylketon bei 90 bis 95 einige Stunden er hitzt. Nach Beendigung der Reaktion fügt man Natronlauge hinzu und erhält nach Ab kühlen die 2.3-Dimethylindol-6-sulfosäure als Natriumsalz. Man erhält ähnlich gute Ausbeuten, wenn man in Alkohol oder in verdünnter Essigsäure arbeitet. Arbeitet plan in Eisessig, so kann man zur Kondensation auch die Salze der Phenylhydrazinsulfo- säuren verwenden.
Process for the preparation of 2,3-dimethylindole-6-sulfonic acid. It has been found that the 2.3 1.) imethylindole-6-sulfonic acid is obtained when m-phenylhydrazine sulfonic acid is condensed with methyl ethyl ketone. The known condensation agents can be used here as condensation agents: for example glacial acetic acid. But you can also work in neutral solution or in weakly acidic, such as dilute acetic acid. The new product crystallizes in the form of the sodium salt in small white crystals. It is said to be used as an intermediate in the manufacture of dyes.
Example: 19 kg of m-phenylhydrazinesulphonic acid in 100 liters of water with 7.5 kg of methyl ethyl ketone at 90 to 95 for a few hours. After the reaction has ended, sodium hydroxide solution is added and, after cooling, the 2,3-dimethylindole-6-sulfonic acid is obtained as the sodium salt. Similar good yields are obtained if one works in alcohol or in dilute acetic acid. If you work in glacial acetic acid, you can also use the salts of phenylhydrazine sulfonic acids for condensation.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE161481X | 1931-03-19 | ||
CH159149T | 1932-02-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH161481A true CH161481A (en) | 1933-04-30 |
Family
ID=25717199
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH161481D CH161481A (en) | 1931-03-19 | 1932-02-18 | Process for the preparation of 2,3-dimethylindole-6-sulfonic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH161481A (en) |
-
1932
- 1932-02-18 CH CH161481D patent/CH161481A/en unknown
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