CH170310A - Process for the preparation of an oxycarbazole carboxylic acid arylamide. - Google Patents
Process for the preparation of an oxycarbazole carboxylic acid arylamide.Info
- Publication number
- CH170310A CH170310A CH170310DA CH170310A CH 170310 A CH170310 A CH 170310A CH 170310D A CH170310D A CH 170310DA CH 170310 A CH170310 A CH 170310A
- Authority
- CH
- Switzerland
- Prior art keywords
- oxycarbazole
- preparation
- carboxylic acid
- acid arylamide
- arylamide
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung eines Oxykarbazolkarbonsäurearylamids. Es wurde gefunden, dass man ein als wertvolles Zwischenprodukt für die Herstellung von Farbstoffen verwendbares Oxykarbazol- karbonsäurearylamid erhält, wenn man eine Verbindung der Formel
EMI0001.0004
in der X einen bei der Reaktion sich abspal tenden Substituenten, zum Beispiel -OH oder Halogen,. bedeutet, mit o-Anisidin umsetzt.
<I>Beispiel:</I> 21,2 gr 9-Methyl-2-ogykarbazol 3-karbon- säure und 12 gr o-Anisidin werden in 500 cm3 Toluol gelöst. Bei<B>60-650</B> lässt man unter Rühren innerhalb '/s Stunde 10,4 gr Phos- phortrichlorid zutropfen, erwärmt dann lang sam zum Sieden und hält das Reaktions produkt 8 Stunden bei dieser Temperatur.
Dann macht man mit Sodalösung alkalisch, bläst mit Wasserdampf alles Flüchtige ab, saugt von dem ausgeschiedenen Arylid ab und wäscht mit Wasser aus. Man erhält das 9-Methyl-2-oxykarbazol-3-karboylamino-2'- methoxybenzol vom F. P. 188-190 . Es stellt ein eyelbstiehiLy weisses Pulver dar.
Process for the preparation of an oxycarbazole carboxylic acid arylamide. It has been found that an oxycarbazole carboxylic acid arylamide which can be used as a valuable intermediate for the preparation of dyes is obtained if a compound of the formula
EMI0001.0004
in which X is a substituent which splits off during the reaction, for example —OH or halogen. means, reacts with o-anisidine.
<I> Example: </I> 21.2 g of 9-methyl-2-ogykarbazole 3-carbonic acid and 12 g of o-anisidine are dissolved in 500 cm3 of toluene. At <B> 60-650 </B>, 10.4 g of phosphorus trichloride are added dropwise with stirring over an hour, then slowly heated to the boil and the reaction product is kept at this temperature for 8 hours.
Then you make alkaline with soda solution, blow off everything volatile with steam, suck off the precipitated arylide and wash out with water. The 9-methyl-2-oxykarbazole-3-carboylamino-2'-methoxybenzene of F.P. 188-190 is obtained. It is an eyelbstiehiLy white powder.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE170310X | 1932-01-12 | ||
CH165824T | 1936-04-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH170310A true CH170310A (en) | 1934-06-30 |
Family
ID=25718153
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH170310D CH170310A (en) | 1932-01-12 | 1932-12-16 | Process for the preparation of an oxycarbazole carboxylic acid arylamide. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH170310A (en) |
-
1932
- 1932-12-16 CH CH170310D patent/CH170310A/en unknown
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