HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2290643Erstellt: 25. Oktober 2026
Thionyl Chloride → 2,5-Dichlorophenylthioglycoloyl chloride
https://huagongshe.com/reaction/2290643
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | 2-(2,5-Dichlorophenyl)-2-mercaptoacetic acid | HCID 22492329 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | 2,5-Dichlorophenylthioglycoloyl chloride | HCID 86741073 | — |
Reaktionsschritte
94.8 g of 2,5-dichlorophenylthioglycolic acid are added to 103.2 g of thionyl chloride. 0.24 g of N-methylpyrrolidone is added, and the mixture is heated at 50° C. for 2 hours and is then cooled down to 0° C. At this temperature the 2,5-dichlorophenylthioglycoloyl chloride formed is then added dropwise in the course of 1 hour to a suspension of 160 g of thionyl chloride and 77.2 g of anhydrous aluminum chloride. The suspension is stirred at 0°-5° C. for 1 hour and is then poured onto a mixture of 1,200 g of ice and 800 ml of water, the resulting mixture is stirred at 80° C. for 1 hour and is then filtered with suction, and the filter cake is washed until neutral and dried in vacuo at 50° C. This gives 88.4 g of 94.5% pure 4,7-dichloro-3-oxythionaphthene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04617403 |
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| Quelldatensatz | uspto-grants-1986_10 |
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| ORD ID | ord-c1165a8de6c545ca9140d070992193a8 |
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| Quellennotiz | uspto-grants-1986_10 |
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