CH167378A - Process for the preparation of 1-acetylamino-2-methyl-4-chlorobenzene-5-sulfonic acid chloride. - Google Patents
Process for the preparation of 1-acetylamino-2-methyl-4-chlorobenzene-5-sulfonic acid chloride.Info
- Publication number
- CH167378A CH167378A CH167378DA CH167378A CH 167378 A CH167378 A CH 167378A CH 167378D A CH167378D A CH 167378DA CH 167378 A CH167378 A CH 167378A
- Authority
- CH
- Switzerland
- Prior art keywords
- acetylamino
- chlorobenzene
- methyl
- sulfonic acid
- acid chloride
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von 1-.Aeetylamino-2-methyl-4-ehlorbenzol- 6-sulfonsäurechlorid. Es wurde gefunden, dass man 1-Acetyl- amino-2-methyl-4-chlorbenzol- 5 -.sulfonsäure- chlorid dadurch erhalten kann, dass man auf 1-Acetylamino-2-methyl-4-chlorbenzol Chlor- sulfonsäure einwirken lässt.
<I>Beispiel:</I> 183,5 Gewichtsteile 1-Acetylamino-2-me- thyl-4-chlorbenzol werden bei 20 bis<B>30'</B> in 1100 Gewichtsteile Chlorsulfonsäure einge tragen und 20 Stunden bei 50 bis 55 ver rührt. Nach dem Abkühlen auf Zimmer temperatur wird das Reaktionsgemisch auf 3000 Gewichtsteile Eis gegeben, das dabei in fester Form sich abscheidende 1-Acetyl- amino-2-methyl- 4-chlorbenzol - 5 - sulfonsäure- chlorid wird von der sauren Brühe abgesaugt und mit kaltem Wasser neutral gewaschen.
Aus Aceton kristallisiert 1-Acetylamino-2- methyl-4-chlorbenzol-5-sulfonsäurechlorid in farblosen Nadeln vom Schmelzpunkt 137 . Es soll als Zwischenprodukt zum Aufbau von Arzneimitteln, Farbstoffen usw. Ver wendung finden.
Process for the preparation of 1-acetylamino-2-methyl-4-chlorobenzene-6-sulfonic acid chloride. It has been found that 1-acetylamino-2-methyl-4-chlorobenzene-5-sulfonic acid chloride can be obtained by allowing chlorosulfonic acid to act on 1-acetylamino-2-methyl-4-chlorobenzene.
<I> Example: </I> 183.5 parts by weight of 1-acetylamino-2-methyl-4-chlorobenzene are entered at 20 to <B> 30 '</B> in 1100 parts by weight of chlorosulfonic acid and for 20 hours at 50 stirred until 55. After cooling to room temperature, the reaction mixture is poured onto 3000 parts by weight of ice, the 1-acetylamino-2-methyl-4-chlorobenzene-5-sulfonic acid chloride which separates out in solid form is filtered off with suction from the acidic broth and mixed with cold Washed neutral with water.
1-Acetylamino-2-methyl-4-chlorobenzene-5-sulfonic acid chloride crystallizes from acetone in colorless needles with a melting point of 137. It is intended to be used as an intermediate in the synthesis of drugs, dyes, etc.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE167378X | 1931-09-09 | ||
CH163888T | 1932-08-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH167378A true CH167378A (en) | 1934-02-15 |
Family
ID=25717875
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH167378D CH167378A (en) | 1931-09-09 | 1932-08-26 | Process for the preparation of 1-acetylamino-2-methyl-4-chlorobenzene-5-sulfonic acid chloride. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH167378A (en) |
-
1932
- 1932-08-26 CH CH167378D patent/CH167378A/en unknown
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