CH224852A - Process for the preparation of an acylated arylsulfonamide. - Google Patents
Process for the preparation of an acylated arylsulfonamide.Info
- Publication number
- CH224852A CH224852A CH224852DA CH224852A CH 224852 A CH224852 A CH 224852A CH 224852D A CH224852D A CH 224852DA CH 224852 A CH224852 A CH 224852A
- Authority
- CH
- Switzerland
- Prior art keywords
- acylated
- arylsulfonamide
- preparation
- dichlorobenzenesulfon
- tolylamide
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Terfahren zur Herstellung eines acylierten Arylsulfonamides. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung eines acylier- ten Arylsulfonamids, welches dadurch ge kennzeichnet ist, dass man 3,4-Dichlorbenzol- sulfon-o-tolylamid oder ein Salz desselben mit einem Acetylierungsmittel behandelt. Die neue Verbindung ist ein farbloses Kristall pulver vom F. 90-91 . Sie dient zur Be kämpfung von Schädlingen der Insekten klasse und der Klein1ebewe1t.
<I>Beispiel:</I> 15 Teile 3,4-Dichlorbenzolsulfon-o-tolyl- amid werden in 100 Volumteilen trockenem Pyridin gelöst, mit 9 Teilen Acetylchlorid versetzt und 24 Stunden auf 80-90 er wärmt. Nach dem Verjagen des Pyridins mit Wasserdampf nimmt man den Rück stand in Äther auf, wäscht mit stark ver dünnter Natronlauge und anschliessend mit Wasser. Nach dem Verdampfen des Äthers erhält man das 3,4-Dichlorbenzolsulfon-o- tolyl-acetamid. Es zeigt nach dem Um kristallisieren aus wässrigem Alkohol einen Schmelzpunkt von 90-91 und besitzt fol gende Konstitution:
EMI0001.0019
The process of making an acylated aryl sulfonamide. The present patent relates to a process for the preparation of an acylated arylsulfonamide, which is characterized in that 3,4-dichlorobenzenesulfone-o-tolylamide or a salt thereof is treated with an acetylating agent. The new compound is a colorless crystal powder from F. 90-91. It is used to control pests of the insect class and small animals.
<I> Example: </I> 15 parts of 3,4-dichlorobenzenesulfon-o-tolylamide are dissolved in 100 parts by volume of dry pyridine, 9 parts of acetyl chloride are added and the mixture is heated to 80-90 for 24 hours. After the pyridine has been chased away with steam, the residue is taken up in ether, washed with very dilute sodium hydroxide solution and then with water. After evaporation of the ether, 3,4-dichlorobenzenesulfon-o-tolyl-acetamide is obtained. After recrystallizing from aqueous alcohol, it has a melting point of 90-91 and has the following constitution:
EMI0001.0019
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH220746T | 1940-02-02 | ||
CH224852T | 1940-02-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH224852A true CH224852A (en) | 1942-12-15 |
Family
ID=25726488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH224852D CH224852A (en) | 1940-02-02 | 1940-02-02 | Process for the preparation of an acylated arylsulfonamide. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH224852A (en) |
-
1940
- 1940-02-02 CH CH224852D patent/CH224852A/en unknown
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