CH167377A - Process for the preparation of 1-acetylamino-2,4-dimethylbenzene-5-sulfonic acid chloride. - Google Patents
Process for the preparation of 1-acetylamino-2,4-dimethylbenzene-5-sulfonic acid chloride.Info
- Publication number
- CH167377A CH167377A CH167377DA CH167377A CH 167377 A CH167377 A CH 167377A CH 167377D A CH167377D A CH 167377DA CH 167377 A CH167377 A CH 167377A
- Authority
- CH
- Switzerland
- Prior art keywords
- dimethylbenzene
- acetylamino
- preparation
- sulfonic acid
- acid chloride
- Prior art date
Links
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Darstellung von 1-Acetylamino-2.4-dimethylbenzol-6-sulfonsäurechlorid. Es wurde gefunden, dass man 1-Acetyl- amino-2. 4-dimethylbenzol-5-sulf onsäurechlo- rid dadurch erhalten kann, dass man auf 1- Acetylamino-2.4-dimethylbenzol Chlorsul- fonsäure einwirken lässt.
<I>Beispiel:</I> 163 Gewichtsteile 1-Acetylamino-2.4-di- methylbenzol werden in 978 Gewichtsteile Chlorsulfonsäure bei 20 bis 30 eingetragen und etwa 20 Stunden bei Zimmertemperatur verrührt. Das Reaktionsgemisch wird dann auf 3000 Gewichtsteile Eis gegeben, das da bei in fester Form sich abscheidene 1-Acetyl- amino-2 . 4-dimethylbenzol-5-sulfonsäurechlo- rid wird von der sauren Brühe abgesaugt und mit kaltem Wasser säurefrei gewaschen.
Aus Aceton kristallisiert 1-Acetylamino-2. 4- dimethylbenzol-5-sulfonsäurechlorid in farb losen vielseitigen Kristallen vom Schmelz punkt 147 . Es soll als Zwischenprodukt zum Aufbau von Farbstoffen, Arzneimitteln usw. Verwendung finden.
Process for the preparation of 1-acetylamino-2,4-dimethylbenzene-6-sulfonic acid chloride. It has been found that 1-acetyl-amino-2. 4-dimethylbenzene-5-sulfonic acid chloride can be obtained by letting chlorosulfonic acid act on 1-acetylamino-2,4-dimethylbenzene.
<I> Example: </I> 163 parts by weight of 1-acetylamino-2,4-dimethylbenzene are added to 978 parts by weight of chlorosulfonic acid at 20 to 30 times and stirred for about 20 hours at room temperature. The reaction mixture is then poured onto 3000 parts by weight of ice, the 1-acetyl-amino-2 which separates out in solid form. 4-dimethylbenzene-5-sulfonic acid chloride is suctioned off from the acidic broth and washed acid-free with cold water.
1-Acetylamino-2 crystallizes from acetone. 4- dimethylbenzene-5-sulfonic acid chloride in colorless, versatile crystals with a melting point of 147. It is intended to be used as an intermediate in the synthesis of dyes, drugs, etc.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE167377X | 1931-09-09 | ||
CH163888T | 1932-08-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH167377A true CH167377A (en) | 1934-02-15 |
Family
ID=25717874
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH167377D CH167377A (en) | 1931-09-09 | 1932-08-26 | Process for the preparation of 1-acetylamino-2,4-dimethylbenzene-5-sulfonic acid chloride. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH167377A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2440117A (en) * | 1944-03-11 | 1948-04-20 | Sun Chemical Corp | Process for preparing sulfonamides |
US2441671A (en) * | 1944-03-11 | 1948-05-18 | Sun Chemical Corp | Process for preparing sulfonamides |
-
1932
- 1932-08-26 CH CH167377D patent/CH167377A/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2440117A (en) * | 1944-03-11 | 1948-04-20 | Sun Chemical Corp | Process for preparing sulfonamides |
US2441671A (en) * | 1944-03-11 | 1948-05-18 | Sun Chemical Corp | Process for preparing sulfonamides |
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