CH307891A - Process for the preparation of a bactericidal salicylanilide. - Google Patents
Process for the preparation of a bactericidal salicylanilide.Info
- Publication number
- CH307891A CH307891A CH307891DA CH307891A CH 307891 A CH307891 A CH 307891A CH 307891D A CH307891D A CH 307891DA CH 307891 A CH307891 A CH 307891A
- Authority
- CH
- Switzerland
- Prior art keywords
- salicylanilide
- bactericidal
- preparation
- methyl
- chloro
- Prior art date
Links
Description
Verfahren zur Herstellung eines bakteriziden Salieylanilides. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines bakteriziden Salicylanilides. Das Verfahren ist dadurch gekennzeichnet, dass man 1 Mol 4-Methyl-5- ehlor-salicylsäure auf 1 Mol 3,4,5-Triehlor- anilin einwirken lässt.
Die erhaltene neue Verbindung, das 4- Methyl - 5 -,chlort-palieylsäure-3',4',5' = triehlor- anilid, schmilzt bei 275-276 . Sie soll als Desinfektionsmittel für nicht arzneiliche Zwecke Verwendung finden.
<I>Beispiel:</I> 47 Teile 4-Methyl-5-chlor-salicylsäure und 50 Teile 3,4,5-Trichlor-anilin werden in 450 Teilen Chlorbenzol gelöst und ein Teil Alu miniumchlorid und 15 Teile Phosphortrichlo- rid zugegeben. Diese Suspension wird so lange zum Sieden erhitzt, bis kein Chlorwasserstoff
EMI0001.0020
mehr <SEP> entweicht, <SEP> was <SEP> nach <SEP> ungefähr <SEP> 2 der Fall ist, Die -eh#orbenzolische Lösung wird dann mit Wasser vermischt und mit Soda brillantalkalisch gestellt.
Das Chlor benzol wird mit Wasserdampf abgeblasen und der Destillationsrückstand, nach dem Abfil- trieren und Trocknen, aus Chlorbenzol um kristallisiert. Das erhaltene 4-Methyl.-5-chlor- salicylsäure-3',4',5'-trichlor-a.nilid schmilzt bei 275-276 .
Process for the preparation of a bactericidal salieylanilide. The present patent relates to a process for the preparation of a bactericidal salicylanilide. The process is characterized in that 1 mol of 4-methyl-5-chlorosalicylic acid is allowed to act on 1 mol of 3,4,5-triehloraniline.
The new compound obtained, 4-methyl-5 -, chloro-palieylic acid-3 ', 4', 5 '= triehloranilide, melts at 275-276. It should be used as a disinfectant for non-medicinal purposes.
<I> Example: </I> 47 parts of 4-methyl-5-chloro-salicylic acid and 50 parts of 3,4,5-trichloro-aniline are dissolved in 450 parts of chlorobenzene and one part of aluminum chloride and 15 parts of phosphorus trichloride are added . This suspension is heated to the boil until there is no hydrogen chloride
EMI0001.0020
more <SEP> escapes, <SEP> what <SEP> is about <SEP> 2 after <SEP>, the -herbenzolic solution is then mixed with water and made brilliantly alkaline with soda.
The chlorobenzene is blown off with steam and the distillation residue is recrystallized from chlorobenzene after it has been filtered off and dried. The 4-methyl.-5-chlorosalicylic acid-3 ', 4', 5'-trichloro-a.nilide obtained melts at 275-276.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH304558T | 1951-12-29 | ||
CH307891T | 1951-12-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH307891A true CH307891A (en) | 1955-06-15 |
Family
ID=25734860
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH307891D CH307891A (en) | 1951-12-29 | 1951-12-29 | Process for the preparation of a bactericidal salicylanilide. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH307891A (en) |
-
1951
- 1951-12-29 CH CH307891D patent/CH307891A/en unknown
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