CH201504A - Process for the preparation of a sulfonic acid chloride. - Google Patents
Process for the preparation of a sulfonic acid chloride.Info
- Publication number
- CH201504A CH201504A CH201504DA CH201504A CH 201504 A CH201504 A CH 201504A CH 201504D A CH201504D A CH 201504DA CH 201504 A CH201504 A CH 201504A
- Authority
- CH
- Switzerland
- Prior art keywords
- acid chloride
- sulfonic acid
- preparation
- chlorobenzene
- ethylsulfone
- Prior art date
Links
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 title claims description 3
- 238000000034 method Methods 0.000 title claims description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 9
- XTHPWXDJESJLNJ-UHFFFAOYSA-N chlorosulfonic acid Substances OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- KEQGZUUPPQEDPF-UHFFFAOYSA-N 1,3-dichloro-5,5-dimethylimidazolidine-2,4-dione Chemical compound CC1(C)N(Cl)C(=O)N(Cl)C1=O KEQGZUUPPQEDPF-UHFFFAOYSA-N 0.000 claims description 2
- 239000000975 dye Substances 0.000 claims description 2
- 239000003960 organic solvent Substances 0.000 claims description 2
- 239000000843 powder Substances 0.000 claims description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 claims 1
- 239000013067 intermediate product Substances 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung eines Sulfonsäurechlorids. Es wurde gefunden, dass man in glatter Reaktion das 1-Chlorbenzol-4-äthylsulfon-2- sulforisäurechlorid erhält, wenn man auf 1- Chlorbenzol-4-äthylsulfon in der Wärme Chlorsulfonsäure einwirken lässt. Das 1-Chlor- benzol-4-äthylsulfon-2-sulfonsäurechlorid bil det ein weisses Pulver, das sich in organischen Lösungsmitteln, wie z. B. in Benzol, löst. Es ist ein wertvolles Zwischenprodukt zur Herstellung von Farbstoffen.
<I>Beispiel:</I> 30 Teile 1-Chlorbenzol-4-äthylsulfon wer den in 300 Teilen Chlorsulfonsäure eingetragen und langsam erwärmt. Bei etwa 90 beginnt bereits die Salzsäureentwicklung, die durch Steigern der Temperatur bis gegen 1401 innert etwa 4 Stunden beendet wird. Durch Eingiessen der erkalteten Masse in Eiswasser erhält man ein festes Produkt, das zur Haupt aache aus dem 1-Chlorbenzol-4-äthylsulfon-2- sulfonsäurechlorid besteht. Es kann gegebe nenfalls durch Kristallisieren aus Benzol, eventuell in Gemisch mit andern Kohlen- wasserstoffen, gereinigt werden. .
Process for the preparation of a sulfonic acid chloride. It has been found that 1-chlorobenzene-4-ethylsulphone-2-sulforic acid chloride is obtained in a smooth reaction if chlorosulphonic acid is allowed to act on 1-chlorobenzene-4-ethylsulphone in the heat. The 1-chloro-benzene-4-ethylsulfone-2-sulfonic acid chloride bil det a white powder that is in organic solvents, such as. B. in benzene, dissolves. It is a valuable intermediate in the manufacture of dyes.
<I> Example: </I> 30 parts of 1-chlorobenzene-4-ethylsulfone are added to 300 parts of chlorosulfonic acid and slowly heated. The evolution of hydrochloric acid begins at around 90 and is terminated within around 4 hours by increasing the temperature up to 1401. By pouring the cooled mass into ice water, a solid product is obtained which mainly consists of 1-chlorobenzene-4-ethylsulfone-2-sulfonic acid chloride. If necessary, it can be purified by crystallizing it from benzene, possibly in a mixture with other hydrocarbons. .
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH201504T | 1936-08-28 | ||
| CH195650T | 1936-08-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH201504A true CH201504A (en) | 1938-11-30 |
Family
ID=25722770
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH201504D CH201504A (en) | 1936-08-28 | 1936-08-28 | Process for the preparation of a sulfonic acid chloride. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH201504A (en) |
-
1936
- 1936-08-28 CH CH201504D patent/CH201504A/en unknown
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